Triethylamine → 4-Butyloxazolidine-2-thione

HRID 1721285

反応式

HRID 1721285 の反応式
[CH3:1][CH2:2][CH2:3][CH2:4][CH:5]([NH2:8])[CH2:6][OH:7].C(N(CC)CC)C.[C:16](Cl)(Cl)=[S:17]>C1COCC1>[CH2:4]([CH:5]1[CH2:6][O:7][C:16](=[S:17])[NH:8]1)[CH2:3][CH2:2][CH3:1]

参加物

5

反応条件

温度
20 °C

実験手順

To a stirred cold solution of DL-2-amino-1-hexanol (1.1 ml) in dry THF (10 ml) was added triethylamine (2.8 ml) followed by dropwise addition of thiophosgene (0.81 ml) in dry THF (9 ml). The mixture was then stirred for 18 h at 20° C., evaporated under reduced pressure and the residue partitioned between water and diethylether. The ether extract was dried with sodium sulphate filtered and evaporated. The residue was dissolved in the minimum of hot 1:1 dimethylether-hexane and crystallised on cooling to give 4-butyloxazolidine-2-thione, mp 71°-2°.

後処理

  1. customevaporated under reduced pressure
  2. customthe residue partitioned between water and diethylether
  3. extractionThe ether extract
  4. dry with materialwas dried with sodium sulphate
  5. filtrationfiltered
  6. customevaporated
  7. dissolutionThe residue was dissolved in the minimum of hot 1:1 dimethylether-hexane
  8. customcrystallised
  9. temperatureon cooling

出典と根拠

ORDレコード
ord-3635554a77c149f9b9b46b6e1e667db9
出典データセット
uspto-grants-1996_04
特許番号
US05510344

関連ノート

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