Methanol → 5,6,7,8-Tetrahydro-4H-thieno[3,2-B]azepine

HRID 1733936ノート

反応式

HRID 1733936 の反応式
[S:1]1[C:10]2[CH2:9][CH2:8][CH2:7][C:6](=O)[NH:5][C:4]=2[CH:3]=[CH:2]1.B.CSC.CO>O1CCCC1>[S:1]1[C:10]2[CH2:9][CH2:8][CH2:7][CH2:6][NH:5][C:4]=2[CH:3]=[CH:2]1

参加物

5

反応条件

温度
0 °C

実験手順

To a mixture of 21.2 g of 5,6,7,8-tetrahydro-4H-thieno[3,2-b]azepin-5-one in 100 ml of tetrahydrofuran under argon, chilled to 0° C. is added 25.2 ml of a 10.0 molar solution of borane-dimethylsulfide in tetrahydrofuran. The solution is stirred at room temperature for 16 hours and is refluxed for 5 hours. The mixture is cooled to room temperature and 85 ml of methanol added dropwise (exotherm). The solvent is removed and 100 ml of methanol is added (2 times) and after each addition the solvent is removed. To the residual solid (dried under vacuum) is added 126 ml of 2N NaOH and the mixture refluxed 3 hours. The mixture is chilled (2 hours) and extracted with dichloromethane. The extract is dried (Na2SO4) and the solvent removed to give 15.4 g of brown solid, m.p. 55°-57° C. A sample (3 g) is sublimed to give 2.6 g of crystals, m.p. 64°-65° C.

後処理

  1. temperatureis refluxed for 5 hours
  2. temperatureThe mixture is cooled to room temperature
  3. customThe solvent is removed
  4. addition100 ml of methanol is added (2 times)
  5. additionafter each addition the solvent
  6. customis removed
  7. customTo the residual solid (dried under vacuum)
  8. additionis added 126 ml of 2N NaOH
  9. temperaturethe mixture refluxed 3 hours
  10. temperatureThe mixture is chilled (2 hours)
  11. extractionextracted with dichloromethane
  12. dry with materialThe extract is dried (Na2SO4)
  13. customthe solvent removed

出典と根拠

ORDレコード
ord-ef7401792efe43188467e539a4ce2a7e
出典データセット
uspto-grants-1996_07
特許番号
US05532235

反応ノート

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