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

N-(o-Nitrobenzyl)ethyl glycine → N-(o-Aminobenzyl)ethyl glycine

HRID 1579987
노트
인쇄 미리보기

반응식

HRID 1579987 반응식
[N+:1]([C:4]1[CH:17]=[CH:16][CH:15]=[CH:14][C:5]=1[CH2:6][CH2:7][CH2:8][NH:9][CH2:10][C:11]([OH:13])=[O:12])([O-])=O.[H][H]>[Pd].C(O)C>[NH2:1][C:4]1[CH:17]=[CH:16][CH:15]=[CH:14][C:5]=1[CH2:6][CH2:7][CH2:8][NH:9][CH2:10][C:11]([OH:13])=[O:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 57139570N-(o-Nitrobenzyl)ethyl glycineHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 57043355N-(o-Aminobenzyl)ethyl glycine수율 77%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

To a solution of 13.0 g. (5.46 × 10-2 moles) of N-(o-nitrobenzyl)ethyl glycine in 200 ml. of absolute ethyl alcohol was added slowly 0.76 g. (5% by weight) of 10% Pd/C catalyst and the mixture placed on a Paar hydrogenator. The mixture was shaken until theoretical hydrogen (16.4 × 10-2 moles) had been absorbed, removed from the Paar and the mixture filtered under suction. The catalyst was washed with ethyl alcohol and the solvent removed in vacuo affording a yellow oil. Purification of the oil was effected by distillation yielding 8.8 g. (77% yield) of a colorless oil; b.p. 124°-126°C. (0.03 mm).

후처리

  1. customhad been absorbed
  2. customremoved from the Paar
  3. filtrationthe mixture filtered under suction
  4. washThe catalyst was washed with ethyl alcohol
  5. customthe solvent removed in vacuo
  6. customaffording a yellow oil
  7. customPurification of the oil
  8. distillationwas effected by distillation
  9. customyielding 8.8 g

출처 및 근거

ORD 기록
ord-fe975d707ff3407482e67275db8a1cc6
출처 데이터셋
uspto-grants-1976_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03932407

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트