Benzene → 3-Benzylamino-1-indanol

HRID 65837ノート

反応式

HRID 65837 の反応式
[C:1]1(=[O:11])[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C:3](=O)[CH2:2]1.C1C=CC=CC=1.[CH2:18]([NH2:25])[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1.[BH4-].[Na+]>CO.O>[CH2:18]([NH:25][CH:3]1[C:4]2[C:9](=[CH:8][CH:7]=[CH:6][CH:5]=2)[CH:1]([OH:11])[CH2:2]1)[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1

参加物

7

実験手順

Stir indan-1,3-dione (7.31 g.), benzene (200 ml.) and benzylamine (5.90 g.) and reflux into a water separator for 6 hours. Cool, filter, and wash the dark solid with ether. Boil the solid with methylene chloride, filter and remove the solvent by boiling and replace with ether. Filter to get 4.51 g. of dark solid. Stir 4.30 g. of this solid with methanol (150 ml.) and add sodium borohydride (12.0 g.) portionwise with stirring over 4 hours. Let the reaction stand at room temperature then evaporate the solvent in vacuo and digest the residue with water and ether. Extract the mixture with ether and wash, dry and evaporate the solvent in vacuo. Recrystallize the residue from cyclohexane-ether to obtain 1.996 g. of the pure free base of the title compound, m.p. 121°-125°.

後処理

  1. temperatureCool
  2. filtrationfilter
  3. washwash the dark solid with ether
  4. filtrationBoil the solid with methylene chloride, filter
  5. customremove the solvent
  6. filtrationFilter
  7. customto get 4.51 g
  8. stirringwith stirring over 4 hours
  9. customat room temperature
  10. customthen evaporate the solvent in vacuo
  11. extractionExtract the mixture with ether
  12. washwash
  13. customdry
  14. customevaporate the solvent in vacuo
  15. customRecrystallize the residue from cyclohexane-ether
  16. customto obtain 1.996 g

出典と根拠

ORDレコード
ord-d5d463a177f34d02b1412d12bf02bce3
出典データセット
uspto-grants-1978_12
特許番号
US04129561

反応ノート

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