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Benzoic acid, 2-[(2-bromophenyl)thio]-5-nitro- → HCID 59797445, 화합물

HRID 33804
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HRID 33804 반응식
[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[S:8][C:9]1[CH:17]=[CH:16][C:15]([N+:18]([O-:20])=[O:19])=[CH:14][C:10]=1[C:11]([OH:13])=O>CS(O)(=O)=O>[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]2[C:3]=1[S:8][C:9]1[CH:17]=[CH:16][C:15]([N+:18]([O-:20])=[O:19])=[CH:14][C:10]=1[C:11]2=[O:13]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 43090919Benzoic acid, 2-[(2-bromophenyl)thio]-5-nitro-

생성물 1

HCID 59797445HCID 59797445, 화합물

시약·촉매·용매 1

HCID 6395Methanesulfonic Acid용매

반응 조건

온도
150 °C

실험 절차

2-(2-Bromo-phenylsulfanyl)-5-nitro-benzoic acid (34 g, 96 mmol) was suspended in methanesulphonic acid (400 ml) and heated at 150° C. The crude mixture was slowly poured onto ice with vigorous stirring and the precipitate formed was filtered. The solid was suspended into water (50 ml) quenched to pH 7-8 with conc. ammonia solution and filtered. The yellow/lime colored solid was dried under vacuum at 50° C. to give the crude title compound, which was used without any further purification (23.09 g, 72%).

후처리

  1. customthe precipitate formed
  2. filtrationwas filtered
  3. customquenched to pH 7-8 with conc. ammonia solution
  4. filtrationfiltered
  5. dry with materialThe yellow/lime colored solid was dried under vacuum at 50° C.

출처 및 근거

ORD 기록
ord-0c3ef924ffbf4510b47d23f689a2f013
출처 데이터셋
uspto-grants-2008_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07429660B2

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