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

Methanol → (1r)-Acetic acid n'-(1-phenyl-but-3-enyl)-hydrazide

HRID 493457
노트
인쇄 미리보기

반응식

HRID 493457 반응식
[CH2:1]([Si]1(Cl)N(C)[C@@H](C)[C@H](C2C=CC=CC=2)O1)[CH:2]=[CH2:3].[CH:18](=[N:25][NH:26][C:27](=[O:29])[CH3:28])[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1.CO>C(Cl)Cl>[C:19]1([C@H:18]([NH:25][NH:26][C:27](=[O:29])[CH3:28])[CH2:3][CH:2]=[CH2:1])[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 887MethanolHCID 246215benzaldehyde N-acetylhydrazoneHCID 10333223(4S,5S)-2-Allyl-2-chloro-3,4-dimethyl-5-phenyl-1-oxa-3-aza-2-silacyclopentane

생성물 1

HCID 12065856(1r)-Acetic acid n'-(1-phenyl-but-3-enyl)-hydrazide수율 80%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

Enantioselective allylation of acetic acid benzylidene-hydrazide (8) to give (1R)-acetic acid N′-(1-phenyl-but-3-enyl)-hydrazide: To a cooled (10° C.) solution of (4S,5S)-2-Allyl-2-chloro-3,4-dimethyl-5-phenyl-[1,3,2]oxazasilolidine (9.90 g, 37.0 mmol) in CH2Cl2 (300 mL) was added acetic acid benzylidene-hydrazide (5.00 g, 30.8 mol) as a solid. The resulting solution was stirred for 16 hours and methanol (40 mL) was then added. After 15 min all volatiles were removed by distillation and the residue was diluted with EtOAc (150 mL) and H2O (500 mL). The phases were separated and the aqueous layer was extracted with EtOAc (2×150 mL). The combined organic layers were washed with H20 and brine, dried (MgSO4), filtered and concentrated. Analysis of the residue by HPLC revealed an ee of 87%. The residue was dissolved in boiling toluene (80 mL) and the solution was then cooled to ambient temperature. Pentane (380 mL) was layered on top of the toluene solution and the resulting biphasic solution was allowed to stand for 16 hours. The resulting crystalline solid precipitate was filtered, washed (pentane:toluene (5:1)) and then dried in vacuo to give 5.04 g (80%) of (1R)-acetic acid N′-(1-phenyl-but-3-enyl)-hydrazide in 98% ee.

후처리

  1. customAfter 15 min all volatiles were removed by distillation
  2. additionthe residue was diluted with EtOAc (150 mL) and H2O (500 mL)
  3. customThe phases were separated
  4. extractionthe aqueous layer was extracted with EtOAc (2×150 mL)
  5. washThe combined organic layers were washed with H20 and brine
  6. dry with materialdried (MgSO4)
  7. filtrationfiltered
  8. concentrationconcentrated
  9. dissolutionThe residue was dissolved
  10. waitto stand for 16 hours
  11. filtrationThe resulting crystalline solid precipitate was filtered
  12. washwashed (pentane:toluene (5:1))
  13. customdried in vacuo

출처 및 근거

ORD 기록
ord-01d0f8eb13f94e938c445ac549cf7f60
출처 데이터셋
uspto-grants-2009_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07534905B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트