Thionyl Chloride → Isoxepac

HRID 262279

반응식

HRID 262279 반응식
[CH2:1]([O:8][C:9]1[CH:14]=[CH:13][C:12]([CH2:15][C:16]([OH:18])=[O:17])=[CH:11][C:10]=1[C:19]([OH:21])=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.S(Cl)(Cl)=O>>[O:21]=[C:19]1[C:7]2[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=2[CH2:1][O:8][C:9]2[CH:14]=[CH:13][C:12]([CH2:15][C:16]([OH:18])=[O:17])=[CH:11][C:10]1=2

참가 물질

3

반응물 2

HCID 24386Thionyl ChlorideHCID 203861514-Benzyloxy-3-carboxyphenylacetic acid

생성물 1

HCID 41448Isoxepac

실험 절차

A sample of 4-benzyloxy-3-carboxyphenylacetic acid is treated with an excess of thionyl chloride at reflux for 2 hours. The excess thionyl chloride is removed in vacuo and the remaining 4-benzyloxy-3-(chlorocarbonyl)phenylacetyl chloride is dissolved in methylene chloride-nitromethane and treated with an equivalent amount of aluminum chloride. The reaction mixture is stirred several hours at room temperature, refluxed for two hours and quenched with dilute hydrochloric acid. The layers are separated, the organic phase dried and evaporated in vacuo to a residue which, on crystallization from isopropyl alcohol yields 6,11-dihydro-11-oxodibenz[b,e]oxepin-2-acetic acid, mp 137°-138°-138° C.

후처리

  1. temperatureat reflux for 2 hours
  2. customThe excess thionyl chloride is removed in vacuo
  3. dissolutionthe remaining 4-benzyloxy-3-(chlorocarbonyl)phenylacetyl chloride is dissolved in methylene chloride-nitromethane
  4. additiontreated with an equivalent amount of aluminum chloride
  5. temperaturerefluxed for two hours
  6. customquenched with dilute hydrochloric acid
  7. customThe layers are separated
  8. customthe organic phase dried
  9. customevaporated in vacuo to a residue which, on crystallization from isopropyl alcohol

출처 및 근거

ORD 기록
ord-97cff358163b4d3499f3f62080dc4e6a
출처 데이터셋
uspto-grants-1979_05
특허 번호
US04153790

연결된 노트

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