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

5-Methyl-4-nitro-thiophene-2-carboxylic acid benzyl ester → 5-Methyl-4-amino-thiophene-2-carboxylic acid benzyl ester

HRID 583761
노트
인쇄 미리보기

반응식

HRID 583761 반응식
[CH2:1]([O:8][C:9]([C:11]1[S:12][C:13]([CH3:19])=[C:14]([N+:16]([O-])=O)[CH:15]=1)=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>O1CCCC1.[Ni]>[CH2:1]([O:8][C:9]([C:11]1[S:12][C:13]([CH3:19])=[C:14]([NH2:16])[CH:15]=1)=[O:10])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 381853005-Methyl-4-nitro-thiophene-2-carboxylic acid benzyl ester

생성물 1

HCID 613104205-Methyl-4-amino-thiophene-2-carboxylic acid benzyl ester수율 107%

시약·촉매·용매 2

HCID 935Nickel촉매HCID 8028Tetrahydrofuran용매

실험 절차

Sponge nickel (0.6 g water wet) was added to a solution of 5-methyl-4-nitro-thiophene-2-carboxylic acid benzyl ester (0.93 g, 3.4 mmol), prepared as described in Step 1 above, in tetrahydrofuran (50 mL), and the mixture was hydrogenated at room temperature under hydrogen atmosphere at a starting pressure of 50 psi. After a reaction time of 2.4 hours, the pressure was released and the mixture filtered. The slurry was rinsed with tetrahydrofuran, and the filtrate was stripped of solvent under reduced pressure, leaving 0.9 g of 5-methyl-4-amino-thiophene-2-carboxylic acid benzyl ester as an oil.

후처리

  1. customprepared
  2. customwas hydrogenated at room temperature under hydrogen atmosphere at a starting pressure of 50 psi
  3. customAfter a reaction time of 2.4 hours
  4. filtrationthe mixture filtered
  5. washThe slurry was rinsed with tetrahydrofuran

출처 및 근거

ORD 기록
ord-6daf8a8dedef405e9b97c0fddcb094f5
출처 데이터셋
uspto-grants-2005_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06924276B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트