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

O-Benzylhydroxylamine → HCID 85993143, 화합물

HRID 271971
노트
인쇄 미리보기

반응식

HRID 271971 반응식
[CH3:1][O:2][C:3](=[O:14])[C:4](=[CH2:13])[CH:5](OC(=O)C)[CH2:6][CH2:7][CH3:8].[CH2:15]([O:22][NH2:23])[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1>C1COCC1>[CH3:1][O:2][C:3](=[O:14])[C:4]([CH2:13][NH:23][O:22][CH2:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)=[CH:5][CH2:6][CH2:7][CH3:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 102313O-BenzylhydroxylamineHCID 103304023-Acetoxy-2-methylenehexanoic acid methyl ester

생성물 1

HCID 85993143HCID 85993143, 화합물수율 212.7%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

A mixture of 3-acetoxy-2-methylenehexanoic acid methyl ester (4.00 g, 20 mmol) and O-benzylhydroxylamine (7.39 g, 60 mmol) in THF (30 mL) is allowed to react at RT under N2 for 2 days. The reaction mixture is concentrated on Rotavap under reduced pressure (20 mbar) until no further solvent distills. The residue liquid is dissolved in ethyl acetate (75 mL) and washed with saturated aqueous sodium bicarbonate solution (50 mL). The ethyl acetate layer is concentrated on Rotavap under reduced pressure (20 mbar) until no further solvent distills to afford a colorless liquid (11.2 g).

후처리

  1. customto react at RT under N2 for 2 days
  2. concentrationThe reaction mixture is concentrated on Rotavap under reduced pressure (20 mbar) until no further solvent
  3. distillationdistills
  4. dissolutionThe residue liquid is dissolved in ethyl acetate (75 mL)
  5. washwashed with saturated aqueous sodium bicarbonate solution (50 mL)
  6. concentrationThe ethyl acetate layer is concentrated on Rotavap under reduced pressure (20 mbar) until no further solvent
  7. distillationdistills

출처 및 근거

ORD 기록
ord-c34d99016fea4b629a649f1050634fe2
출처 데이터셋
uspto-grants-2008_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07452999B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트