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4-Bromobenzoic acid → 4-Bromo-3-(chlorosulfonyl)benzoic acid

HRID 516804
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HRID 516804 반응식
[Br:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[CH:4][CH:3]=1.[Cl:11][S:12](O)(=[O:14])=[O:13]>>[Br:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[CH:4][C:3]=1[S:12]([Cl:11])(=[O:14])=[O:13]
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참가 물질

3

반응물 2

HCID 114644-Bromobenzoic acidHCID 24638Chlorosulfonic acid

생성물 1

HCID 37373734-Bromo-3-(chlorosulfonyl)benzoic acid수율 79.5%

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온도
130 °C

실험 절차

4-Bromobenzoic acid (10 g, 49.75 mmol) was added portion wise to chlorosulfonic acid (25 ml, 373.13 mmol) at 0° C. The mixture was heated to 130° C. for 10 hours, until complete consumption of the starting material was observed by LCMS. The reaction mixture was allowed to cool down to ambient temperature, then added drop wise to an ice/water mixture (500 ml). The precipitate was filtered and washed with cold water (2×100 ml). The solid recovered was dissolved in diethyl ether, the solution then dried over sodium sulphate, filtered and concentrated in vacuo to afford the expected product as a beige solid (11.85 g, 79% yield); δH (400 MHz, DMSO) 8.45 (1H, d, 1.7 Hz), 7.72 (1H, d, 2.2 Hz), 7.71 (1H, s); TR=2.08 min.

후처리

  1. temperatureto cool down to ambient temperature
  2. filtrationThe precipitate was filtered
  3. washwashed with cold water (2×100 ml)
  4. customThe solid recovered
  5. dissolutionwas dissolved in diethyl ether
  6. dry with materialthe solution then dried over sodium sulphate
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-566f219865e94fb0a07880cdfd5a93a0
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09115064B2

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