홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Isobutyraldehyde → 2-Carboethoxycarbonyl-4-methyl pentanoic acid

HRID 273837
노트
인쇄 미리보기

반응식

HRID 273837 반응식
[CH3:1][C:2]([CH3:5])([O-])[CH3:3].[K+].C(=[O:11])C(C)C.[C:12]([O:21]CC)(=[O:20])[CH2:13][CH2:14][C:15]([O:17][CH2:18][CH3:19])=[O:16]>C(O)(C)(C)C>[C:15]([C:14]([CH:13]([CH2:1][CH:2]([CH3:5])[CH3:3])[C:12]([OH:21])=[O:20])=[O:11])([O:17][CH2:18][CH3:19])=[O:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6561IsobutyraldehydeHCID 31249Diethyl SuccinateHCID 23665647Potassium tert-butoxide

생성물 1

HCID 537313912-Carboethoxycarbonyl-4-methyl pentanoic acid

시약·촉매·용매 1

HCID 6386tert-Butanol용매2회

실험 절차

Potassium t-butoxide, 24.7 g (0.35M), was dissolved in 200 ml of refluxing t-butanol. A mixture of isobutyraldehyde, 18.2 ml (0.20M) and diethyl succinate 41.55 ml (0.25M) was added to the t-butanol solution over 30 min. The reaction mixture was stirred under reflux, for 2 h. The solvent was removed from the reaction mixture by evaporation under reduced pressure and acidified with 2N HCl. The product was extracted with ethyl ether, Et2O (3×200 ml). The ether solution was washed with water (3×200 ml); and the product was extracted with 10% Na2CO3 (4×200 ml). The solution was acidified with conc. HCl solution and the product was isolated by extraction with Et2O (4×150 ml). The ether layer was washed with water, dried over sodium sulfate, and evaporated. The remaining oil was dissolved in ethanol (300 ml) and hydrogenated in the presence of 10% palladium on charcoal (3.0 g). The resultant mixture was filtered through Celite and the solvent was evaporated to yield 38.04 g 2-carboethoxycarbonyl-4-methyl pentanoic acid as a mixture of isomers in the form of an oil. The isolated monoethyl ester was further purified on silica gel by flash chromatography using as eluent mixture ethyl acetate:hexane:acetic acid (1:10:0.05, v/v).

후처리

  1. temperatureunder reflux, for 2 h
  2. customThe solvent was removed from the reaction mixture by evaporation under reduced pressure
  3. extractionThe product was extracted with ethyl ether, Et2O (3×200 ml)
  4. washThe ether solution was washed with water (3×200 ml)
  5. extractionand the product was extracted with 10% Na2CO3 (4×200 ml)
  6. customthe product was isolated by extraction with Et2O (4×150 ml)
  7. washThe ether layer was washed with water
  8. dry with materialdried over sodium sulfate
  9. customevaporated
  10. dissolutionThe remaining oil was dissolved in ethanol (300 ml) and hydrogenated in the presence of 10% palladium on charcoal (3.0 g)
  11. filtrationThe resultant mixture was filtered through Celite
  12. customthe solvent was evaporated

출처 및 근거

ORD 기록
ord-7315760ec09d499eaa55c59d396002f7
출처 데이터셋
uspto-grants-1995_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05387610

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트