Thioglycolic Acid → HCID 178526169、化合物

HRID 22272

反応式

HRID 22272 の反応式
[Br:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH2:5]Br.[C:10](O)(=O)[CH2:11][SH:12].[OH-:15].[K+]>C(O)C.O>[Br:1][C:2]1[CH:3]=[C:4]([CH2:5][CH2:10][C:11]([OH:15])=[S:12])[CH:7]=[CH:8][CH:9]=1

参加物

6

実験手順

To a solution of 3-bromobenzyl bromide (23.75 g, 90 mmol) and thioglycolic acid (11.42 g, 120 mmol) in ethanol (150 mL) was added potassium hydroxide (14.24 g, 250 mmol) in water (50 mL). The reaction was heated at reflux for 3.5 h, cooled and the ethanol was evaporated. The residue was quenched with water (100 mL) and the mixture was extracted with ether (50 mL). The aqueous layer was acidified to pH 1 with concentrated hydrochloric acid, extracted with ethyl acetate (2×100 mL) and the organic phase was dried. Evaporation of the solvent followed by washing of the residue with hexane afforded 3-bromophenylmethylthioacetic acid as a white solid (92%), mp 90°-91° C.: 1H NMR (CDCl3) δ3.10 (s, 2H), 3.82 (s, 2H), 7.20-7.29 (m, 2H), 7.39-7.42 (dd, 1H), 7.52 (d, 1H); IR (KBr) 1706 cm-1 ; Mass spectrum m/z 280 (M+NH4); Anal. calcd. for C9H9O2SBr: C 41.39, H 3.47, S 12.28; Found C 41.43, H 3.49, S 12.10.

後処理

  1. temperatureThe reaction was heated
  2. temperatureat reflux for 3.5 h
  3. temperaturecooled
  4. customthe ethanol was evaporated
  5. customThe residue was quenched with water (100 mL)
  6. extractionthe mixture was extracted with ether (50 mL)
  7. extractionextracted with ethyl acetate (2×100 mL)
  8. customthe organic phase was dried
  9. customEvaporation of the solvent
  10. washby washing of the residue with hexane

出典と根拠

ORDレコード
ord-cd69c48598cb494798ccebfd7e04088b
出典データセット
uspto-grants-1995_06
特許番号
US05428040

関連ノート

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