Réaction #476528

Équation de réaction

ethanethiol

triethylamine

1-chloroethyl chloroformate

→

title compound ( 2 )

Rendement 89.0%

O-(1-Chloroethyl) S-Ethyl Thiocarbonate

Rendement 89.0%

Solvants

diethyl ether

diethyl ether

Conditions de réaction

Traitement

1. 1
   AutreThe reaction mixture was removed from the ice bath
2. 2
   AutreTriethylamine hydrochloride was removed by filtration
3. 3
   Concentrationthe filtrate concentrated under reduced pressure
4. 4
   workup.DISTILLATIONthe residue purified by vacuum distillation (67-68° C. at 240 mTorr)

Mode opératoire

A solution of 1-chloroethyl chloroformate (71.5 g, 0.5 mol) in diethyl ether (600 mL) was cooled to 0-4° C. in an ice-water bath and a solution of ethanethiol (37 mL, 0.5 mol) and triethylamine (69.3 mL, 0.5 mol) in diethyl ether (200 mL) was added dropwise over 1 h. The reaction mixture was removed from the ice bath and stirred at ambient temperature for 4 h. Triethylamine hydrochloride was removed by filtration, the filtrate concentrated under reduced pressure and the residue purified by vacuum distillation (67-68° C. at 240 mTorr) to afford the title compound (2) as a colorless liquid (75 g, 89%). 1H NMR (CDCl3, 400 MHz): δ 1.35 (t, 3H), 1.8 (d, 3H), 2.9 (dq, 2H), 6.6 (q, 1H).

Source