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

Hydrochloric Acid → 3,3'-Diaminobenzidine

HRID 1673071
노트
인쇄 미리보기

반응식

HRID 1673071 반응식
O.O.Cl[Sn]Cl.Cl.[N+:7]([C:10]1[CH:11]=[C:12]([C:17]2[CH:23]=[CH:22][C:20]([NH2:21])=[C:19]([N+:24]([O-])=O)[CH:18]=2)[CH:13]=[CH:14][C:15]=1[NH2:16])([O-])=O>>[NH2:7][C:10]1[CH:11]=[C:12]([C:17]2[CH:23]=[CH:22][C:20]([NH2:21])=[C:19]([NH2:24])[CH:18]=2)[CH:13]=[CH:14][C:15]=1[NH2:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 313Hydrochloric AcidHCID 61436Stannous chloride dihydrateHCID 31067203,3'-Dinitrobenzidine

생성물 1

HCID 70713,3'-Diaminobenzidine수율 70%

실험 절차

A 50 ml single neck round bottomed flask equipped with condenser, and stirring magnetic bar were placed SnCl2.2H2O (6 g, 26.5 mmol) and 12.5 ml concentrated hydrochloric acid and reaction mixture was stirred and than 3,3′-dinitrobenzidine formula 2 where in R═CH3 (DNB) (1.176 g, 4 mmol) was added in small portions over 15 minute to maintain the reaction temperature less than 60° C. The thick slurry was then stirred for additional 2 hours at 40° C. to complete the reduction. The salt of the tetramine was precipitated out, which was neutralized with cold 10% NaOH solution and the solid filtered out, washed with water dried under vacuum to give 3,3′-diaminobenzidine (DAB) in 70% yield (0.655 g).

후처리

  1. customA 50 ml single neck round bottomed flask equipped with condenser
  2. additionwas added in small portions over 15 minute
  3. temperatureto maintain the reaction temperature less than 60° C
  4. stirringThe thick slurry was then stirred for additional 2 hours at 40° C.
  5. customThe salt of the tetramine was precipitated out
  6. filtrationthe solid filtered out
  7. washwashed with water
  8. customdried under vacuum

출처 및 근거

ORD 기록
ord-5d9ce111e75f438d893a8ebe38e68ec9
출처 데이터셋
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07999112B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트