Home Cart Sign in  
Chemical Structure| 39662-63-0 Chemical Structure| 39662-63-0

Structure of 39662-63-0

Chemical Structure| 39662-63-0

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • {[ item.pr_size ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of [ 39662-63-0 ]

CAS No. :39662-63-0
Formula : C6H11NO2
M.W : 129.16
SMILES Code : O=C1NC(OCC)CC1
MDL No. :MFCD03426969

Safety of [ 39662-63-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362-P403+P233-P501

Application In Synthesis of [ 39662-63-0 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 39662-63-0 ]

[ 39662-63-0 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 39662-63-0 ]
  • [ 108-95-2 ]
  • [ 207989-87-5 ]
YieldReaction ConditionsOperation in experiment
With conc. sulphuric acid; In cyclohexane; acetic acid; ethyl acetate; Example XI-2 At 0 C., 12.9 g of gamma-ethoxy-gamma-butyrolactam, 10 ml of conc. sulphuric acid and 90 ml of glacial acetic acid were initially charged and admixed, a little at a time, with a total of 18.8 g of phenol. After thawing, the mixture was stirred at room temperature for 2 days. For work-up, the mixture was poured onto ice and extracted three times with ethyl acetate, and the combined extracts were washed once each with water and saturated sodium chloride solution, dried and concentrated. After some time, gamma-2-hydroxyphenyl-gamma-butyrolactam (XI-2b) of melting point 220 C. (6.4 g, 36% of theory) crystallized from the aqueous phase. The residue obtained after concentration was stirred with a 1:1 mixture of cyclohexane/ethyl acetate and gave, after filtration with suction, 4.65 g of gamma-4-hydroxyphenyl-gamma-butyrolactam (XI-2a) of melting point 183 C. The filtrate was concentrated. A further 3.35 g (total: 45% of theory) of gamma-4-hydroxyphenyl-gamma-butyrolactam were obtained by recrystallization from dichloromethane/hexane.
With conc. sulphuric acid; In cyclohexane; acetic acid; ethyl acetate; Example X-2 12.9 g of gamma-ethoxy-gamma-butyrolactam, 10 ml of conc. sulphuric acid and 90 ml of glacial acetic acid were initially charged at 0 C. and admixed a little at a time with a total of 18.8 g of phenol. After thawing, the mixture was stirred at room temperature for 2 days. For work-up, the mixture was poured onto ice and extracted three times with ethyl acetate, and the combined extracts were washed once each with water and saturated sodium chloride solution, dried and evaporated. After some time, gamma-2-hydroxyphenyl-gamma-butyrolactam (X-2b) of melting point 220 C. (6.4 g 36% of theory) crystallized form the aqueous phase. The evaporation residue was stirred with a 1:1 mixture of cyclohexane/ethyl acetate and gave, after filtration with suction, 4.65 g of gamma4-hydroxyphenyl-gamma-butyrolactam (X-2a) of melting point 183 C. The filtrate was concentrated. Recrystallization from dichloromethane/hexane gave a further 3.35 g (total: 45% of theory) of gamma-4-hydroxyphenyl-gamma-butyrolactam.
With conc. sulphuric acid; In cyclohexane; acetic acid; ethyl acetate; Example XI-2 At 0 C., 12.9 g of gamma-ethoxy-gamma-butyrolactam, 10 ml of conc. sulphuric acid and 90 ml of glacial acetic acid were initially charged and admixed, a little at a time, with a total of 18.8 g of phenol. After thawing, the mixture was stirred at room temperature for 2 days. For work-up, the mixture was poured onto ice and extracted three times with ethyl acetate, and the combined extracts were washed once each with water and saturated sodium chloride solution, dried and concentrated. After some time, gamma-2-hydroxyphenyl-y-butyrolactam (XI-2b) of melting point 220 C. (6.4 g, 36% of theory) crystallized from the aqueous phase. The residue obtained after concentration was stirred with a 1:1 mixture of cyclohexane/ethyl acetate and gave, after filtration with suction, 4.65 g of gamma-4-hydroxyphenyl-gamma-butyrolactam (XI-2a) of melting point 183 C. The filtrate was concentrated. A further 3.35 g (total: 45% of theory) of gamma-4-hydroxyphenyl-gamma-butyrolactam were obtained by recrystallization from dichloromethane/hexane.
  • 2
  • [ 39662-63-0 ]
  • [ 7664-93-9 ]
  • [ 108-95-2 ]
  • [ 207989-87-5 ]
YieldReaction ConditionsOperation in experiment
In cyclohexane; acetic acid; ethyl acetate; EXAMPLE XI-2 12.9 g of gamma-ethoxy-gamma-butyrolactam, 10 ml of concentrated sulphuric acid and 90 ml of glacial acetic acid were charged initially at 0 C. and admixed a little at a time with a total of 18.8 g of phenol. After thawing, the mixture was stirred at room temperature for 2 days. For work-Up, the mixture was poured onto ice and extracted three times with ethyl acetate, and the combined extracts were washed once with water and once with saturated aqueous sodium chloride solution, dried and evaporated. After some time, gamma-2-hydroxyphenyl-gamma-butyrolactam (XI-2b) of melting point 220 C. (6.4 g, 36% of theory) crystallized from the aqueous phase. The residue obtained on evaporation was stirred with 1:1 mixture of cyclohexane/ethyl acetate and afforded on filtration with suction 4.65 g of gamma-4-hydroxyphenyl-gamma-butyrolactam (XI-2a) of melting point 183 C. The filtrate was evaporated. Recrystallization from dichloromethane/hexane gave a further 3.35 g (total 45% of theory) of gamma-4-hydroxyphenyl-gamma-butyrolactam.
 

Historical Records