Cyclohexylamine → HCID 15730054, compound

HRID 326566Notes

Reaction equation

HRID 326566 reaction equation
[SH:1][CH2:2][C:3]([O:5]CC)=O.[CH:8]1([NH2:14])[CH2:13][CH2:12][CH2:11][CH2:10][CH2:9]1>C(O)C>[CH:8]1([NH:14][C:3](=[O:5])[CH2:2][SH:1])[CH2:13][CH2:12][CH2:11][CH2:10][CH2:9]1

Participants

4

Procedure

A solution of ethyl 2-mercaptoacetate (12 g) and cyclohexylamine (29.7 g) in ethanol (50 ml) was allowed to stand at ambient temperature for 72 hours, and was then refluxed for 6 hours. The solvent was evaporated and the residue dissolved in ethyl acetate (200 ml). The solution was washed sequentially with 2M HCl (3×50 ml), water (2×50 ml) and brine (50 ml) and the solvent removed in vacuo. The crude product was purified by chromatography on silica (eluting with dichloromethane/methanol 99:1 v/v) to give N-cyclohexyl-2-mercaptoacetamide as low-melting tan crystals; NMR: 1.0-2.0(complex, 11H, cyclohexyl-CH2 and SH), 3.2(d, 2H, CH2), 3.6-3.9(m, 1H, cyclohexyl-CH), 6.4-6.9(broad d, 1H, NH); m/e 174 (M+H)+.

Workup

  1. temperaturewas then refluxed for 6 hours
  2. customThe solvent was evaporated
  3. dissolutionthe residue dissolved in ethyl acetate (200 ml)
  4. washThe solution was washed sequentially with 2M HCl (3×50 ml), water (2×50 ml) and brine (50 ml)
  5. customthe solvent removed in vacuo
  6. customThe crude product was purified by chromatography on silica (eluting with dichloromethane/methanol 99:1 v/v)

Sources & evidence

ORD record
ord-2a3407eb447748f28bfda5b4447830a2
Source dataset
uspto-grants-1993_12
Patent number
US05270311

Reaction notes

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