Home Cart Sign in  
Chemical Structure| 42807-86-3 Chemical Structure| 42807-86-3

Structure of 42807-86-3

Chemical Structure| 42807-86-3

*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 [ 42807-86-3 ]

CAS No. :42807-86-3
Formula : C11H23NO2
M.W : 201.31
SMILES Code : CC(C)(C)OC([C@@H](NC)CC(C)C)=O

Safety of [ 42807-86-3 ]

Application In Synthesis of [ 42807-86-3 ]

* 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 [ 42807-86-3 ]

[ 42807-86-3 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 3060-46-6 ]
  • [ 115-11-7 ]
  • [ 42807-86-3 ]
  • 2
  • [ 3060-46-6 ]
  • [ 7664-93-9 ]
  • [ 115-11-7 ]
  • [ 42807-86-3 ]
YieldReaction ConditionsOperation in experiment
19.41 g (94%) With potassium hydroxide; In 1,4-dioxane; water; Step 1: The preparation of (S)-2-(4-tert-butylbenzyl-methyl-amino)-4-methyl-pentanoic acid (IIc) STR30 Step i: (S)-4-Methyl-2-methylamino-pentanoic acid (15 g, 103 mmol) was dissolved in dioxane (100 mL), cooled to 0 C., then treated with H2 SO4 (10 mL) and isobutylene (100 mL). The mixture was stirred and allowed to come to room temperature over 1 hour. The reaction was vented and poured into a rapidly stirred mixture of KOH (20.7 g) in water, ice, and ether. The solution was filtered, and more ether was added. The organic layer was dried over Na2 SO4 and concentrated to give 19.41 g (94%) of (S)4-methyl-2-methylamino-pentanoic acid tert-butyl ester. MS: 202 (M+1 for C11 H23 N1 O2); TLC SiO2, Rf 0.52 (10% MeOH/CH2 Cl2).
  • 3
  • [ 66866-69-1 ]
  • [ 115-11-7 ]
  • [ 42807-86-3 ]
YieldReaction ConditionsOperation in experiment
With sulfuric acid; In 1,4-dioxane; dichloromethane; at 0 - 20℃; for 18h;Sealed tube; 2-Methylpropene (25 g, 446 mmol) was bubbled into DCM (50 mL) at -78C. Then the 2- methylpropene solution was added to a solution of <strong>[66866-69-1](S)-4-methyl-2-(methylamino)pentanoic acid hydrochloride</strong> (500 mg, 2.75 mmol) and H2SO4 (3.68 g, 2 mL, 37.5 mmol) in dioxane (20 mL) at 0C. The reaction mixture was stirred at room temperature for 18 hrs in a sealed tube. The reaction solution was poured into an ice cold aqueous KOH solution (8.4 g in water (30mL)) and the resulting mixture was extracted with DCM (50 mL) twice. The combined organic layer was washed with brine (30 mL) twice, dried over Na2S04 and concentrated in vacuo to afford the crude product ie/t-butyl (2S)-4-methyl-2-(methylamino)pentanoate (Compound AT-1) as a light yellow oil.
With sulfuric acid; In 1,4-dioxane; dichloromethane; at -78 - 20℃; for 18h;Sealed tube; 2-Methylpropene (25 g, 446 mmol) was bubbled into DCM (50 mL) at -78C. Then the 2-methylpropene solution was added to a solution of (S)-4-methyl-2- (methylamino)pentanoic acid hydrochloride (500 mg, 2.75 mmol) and H2S04 (3.68 g, 2 mL, 37.5 mmol) in dioxane (20 mL) at 0C. The reaction mixture was stirred at roomtemperature for 18 hrs in a sealed tube. The reaction solution was poured into an ice coldaqueous KOH solution (8.4 g in water (3OmL)) and the resulting mixture was extractedwith DCM (50 mL) twice. The combined organic layer was washed with brine (30 mL)twice, dried over Na2SO4 and concentrated in vacuo to afford the crude product tert-butyl(2S)-4-methyl-2-(methylamino)pentanoate (Compound AT-i) as a light yellow oil.
With sulfuric acid; In 1,4-dioxane; dichloromethane; at 0 - 20℃; for 18h;Sealed tube; 2-Methylpropene (25 g, 446 mmol) was bubbled into DCM (50 mL) at -78 C. Then the 2-methylpropene solution was added to a solution of <strong>[66866-69-1](S)-4-methyl-2-(methylamino)pentanoic acid hydrochloride</strong> (500 mg, 2.75 mmol) and H2SO4 (3.68 g, 2 mL, 37.5 mmol) in dioxane (20 mL) at 0 C. The reaction mixture was stirred at room temperature for 18 hrs in a sealed tube. The reaction solution was poured into an ice cold aqueous KOH solution (8.4 g in water (30 mL)) and the resulting mixture was extracted with DCM (50 mL) twice. The combined organic layer was washed with brine (30 mL) twice, dried over Na2SO4 and concentrated in vacuo to afford the crude product tert-butyl (2S)-4-methyl-2-(methylamino)pentanoate (Compound AT-1) as a light yellow oil.
 

Historical Records