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

HRID 516804
ノート
印刷プレビュー

反応式

HRID 516804 の反応式
[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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

HCID 114644-Bromobenzoic acidHCID 24638Chlorosulfonic acid

生成物 1

HCID 37373734-Bromo-3-(chlorosulfonyl)benzoic acid収率 79.5%

反応条件

温度
130 °C

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-566f219865e94fb0a07880cdfd5a93a0
出典データセット
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09115064B2

反応ノート

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