Methanol → Methyl 4,10-dihydro-10-oxothieno[3,2-c][1]benzoxepin-8-acetate

HRID 866769노트

반응식

HRID 866769 반응식
[O:1]=[C:2]1[C:8]2[CH:9]=[C:10]([CH2:13][C:14]([OH:16])=[O:15])[CH:11]=[CH:12][C:7]=2[O:6][CH2:5][C:4]2[CH:17]=[CH:18][S:19][C:3]1=2.S(=O)(=O)(O)O.[CH3:25]O>>[O:1]=[C:2]1[C:8]2[CH:9]=[C:10]([CH2:13][C:14]([O:16][CH3:25])=[O:15])[CH:11]=[CH:12][C:7]=2[O:6][CH2:5][C:4]2[CH:17]=[CH:18][S:19][C:3]1=2

참가 물질

4

실험 절차

A mixture of 0.70 g of 4,10-dihydro-10-oxothieno[3,2-c][1]benzoxepin-8-acetic acid (Example 1), 8 ml of concentrated sulfuric acid, and 150 ml of methanol is refluxed for 16 hours. The reaction mixture is concentrated in vacuo, diluted with water and extracted with benzene. The combined benzene extracts are washed with 5% sodium hydroxide and water, dried, filtered and concentrated in vacuo to an oil which solidifies upon standing. The solid is recyrstallized from methanol to provide light yellow crystals, mp 80°-81° C. of methyl 4,10-dihydro-10-oxothieno[3,2-c][1]benzoxepin-8-acetate.

후처리

  1. temperatureis refluxed for 16 hours
  2. concentrationThe reaction mixture is concentrated in vacuo
  3. additiondiluted with water
  4. extractionextracted with benzene
  5. washThe combined benzene extracts are washed with 5% sodium hydroxide and water
  6. customdried
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo to an oil which

출처 및 근거

ORD 기록
ord-be1e5355f9a842979c8002f8a1b11f61
출처 데이터셋
uspto-grants-1978_07
특허 번호
US04101559

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