Home Cart Sign in  
Chemical Structure| 5431-93-6 Chemical Structure| 5431-93-6

Structure of 5431-93-6

Chemical Structure| 5431-93-6

*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 [ 5431-93-6 ]

CAS No. :5431-93-6
Formula : C8H13NO4
M.W : 187.19
SMILES Code : CC(C(NC(C)=O)C(OCC)=O)=O
MDL No. :MFCD09761211

Safety of [ 5431-93-6 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 5431-93-6 ]

* 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 [ 5431-93-6 ]

[ 5431-93-6 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 5431-93-6 ]
  • [ 92901-94-5 ]
YieldReaction ConditionsOperation in experiment
Example 1.6Dimethyloxazolyl Methanol; Sodium nitrite (12.2 g, 0.18 mol) in water was added dropwise to a solution of ethyl acetoacetate (19.5 mL, 0.15 mol) in glacial acetic acid at r.t. for 1 h. The resulting mixture was stirred for further 1 h at r.t, 80 mL of water added, and stirring continued for 2 h. The reaction mixture was extracted with ether for three times, washed with aqueous Na HCO3, water and brine. The organic layer was dried, concentrated to afford the crude product. Without further purification, the crude product (6.5 g, 40.8 mmol) in a mixture of acetic anhydrous (19.3 mL, 0.21 mol), acetic acid (58 mL), and 210 mg of Pd/C (10% w/w) was hydrogenated at 50 Psi pressure for 1.5 h. The catalyst and solvent were removed and the residue was triturated with hexanes to give ethyl N-acetylacetoacetate as solid, m.p. 38-40 C.The above solid product (3.3 g, 17.6 mmol) was treated with thionyl chloride (1.3 mL, 17.6 mmol) in dry benzene at r.t. The mixture was warmed to 30 C. for 1 h, and for 30 min under water-pump vacuum. The residue was diluted with EtOAc and washed with aqueous NaHCO3, water, and brine. The organic layer was dried, concentrated to give the crude product as a brown oil, which was further reduced by LAH to provide the desired alcohol as a light yellow solid. 1H-NMR: (300 MHz, CDCl3), δ: 4.51 (s, 2H); 2.58 (s, 3H); 2.43 (s, 3H), 2.31 (s, 3H).
The above solid product (3.3 g, 17.6 mmol) was treated with thionyl chloride (1.3 mL, 17.6 mmol) in dry benzene at r.t. The mixture was warmed to 30 0C for 1 h, and for 30 min under water-pump vacuum. The residue was diluted with EtOAc and washed with aqueous NaHCO3, water, and brine. The organic layer was dried, concentrated to give the crude product as a brown oil, which was further reduced by LAH to provide the desired alcohol as a light yellow solid. 1H-NMR: (300 MHz, CDCl3), δ: 4.51 (s, 2 H); 2.58 (s, 3 H); 2.43 (s, 3 H), 2.31 (s, 3 H).
  • 2
  • [ 5431-93-6 ]
  • [ 23000-14-8 ]
  • 3
  • [ 5431-93-6 ]
  • [ 2632-14-6 ]
  • C18H23NO5 [ No CAS ]
  • 4
  • [ 5431-93-6 ]
  • [ 2632-14-6 ]
  • (3aSR,5RS,6aSR)-ethyl 5-(4-ethylphenyl)-2,3a-dimethyl-3a,5,6,6a-tetrahydrofuro[3,2-d]oxazole-6a-carboxylate [ No CAS ]
 

Historical Records