Thioglycolic Acid → HCID 178526169, 화합물

HRID 22272

반응식

HRID 22272 반응식
[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

참가 물질

6

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-cd69c48598cb494798ccebfd7e04088b
출처 데이터셋
uspto-grants-1995_06
특허 번호
US05428040

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