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2-Aminothiophenol → 2,4-di-t-butyl-1-hydroxy-10H-phenothiazine

HRID 231052
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인쇄 미리보기

반응식

HRID 231052 반응식
[C:1]([C:5]1[C:6](=[O:16])[C:7](=O)[CH:8]=[C:9]([C:11]([CH3:14])([CH3:13])[CH3:12])[CH:10]=1)([CH3:4])([CH3:3])[CH3:2].[NH2:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][C:19]=1[SH:24]>CO>[C:1]([C:5]1[CH:10]=[C:9]([C:11]([CH3:14])([CH3:13])[CH3:12])[C:8]2[S:24][C:19]3[C:18](=[CH:23][CH:22]=[CH:21][CH:20]=3)[NH:17][C:7]=2[C:6]=1[OH:16])([CH3:4])([CH3:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 87132-AminothiophenolHCID 769153,5-Di-tert-butyl-1,2-benzoquinone

생성물 1

HCID 138820352,4-di-t-butyl-1-hydroxy-10H-phenothiazine

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a solution of 3,5-di-t-butyl-1,2-benzoquinone (2.2 q) in methanol (15 ml) cooled in an ice bath was added 2-aminothiophenol (1.38 g) and the mixture was stirred for 2 hours. A solid precipitate was filtered off and crystallized from heptane to yield the title compound m.p. 202°-212° (dec.). From the methanol filtrate there was obtained, after chromatography and crystallization, an additional crop of the title compound.

후처리

  1. filtrationA solid precipitate was filtered off
  2. customcrystallized from heptane

출처 및 근거

ORD 기록
ord-03b6e877bf1b4ebcb605976dc3437dd0
출처 데이터셋
uspto-grants-1989_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04845083

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