Triethylamine → 4-Butyloxazolidine-2-thione

HRID 1721285

Reaction equation

HRID 1721285 reaction equation
[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]

Participants

5

Conditions

Temperature
20 °C

Procedure

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°.

Workup

  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

Sources & evidence

ORD record
ord-3635554a77c149f9b9b46b6e1e667db9
Source dataset
uspto-grants-1996_04
Patent number
US05510344

Linked notes

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