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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1284212Generated: November 2, 2026

4-Chlorobenzyl mercaptan → HCID 54340232, compound

https://huagongshe.com/reaction/1284212

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobenzyl mercaptanHCID 80409—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 54043382HCID 54043382—
Solventtert-ButanolHCID 6386—
ProductHCID 54340232HCID 54340232—

Reaction Steps

8.1 g (0.05 mol) of 1-chloro-5-isopropoxy-2-pentene are added dropwise at 20-25° during the course of 10 minutes and while stirring to a solution of 7.9 g (0.05 mol) of 4-chloro-benzylmercaptan and 5.6 g (0.05 mol) of potassium tert.butoxide in 150 cc of tert.butanol. The solution which is rendered turbid during the addition is stirred at 60° during the course of 1 hour and is then cooled and filtered. The solvent is distilled off at reduced pressure, the residue is dissolved in ether and the ether solution is washed with saturated salt solution. The ether phase is dried with sodium sulphate and then the ether is distilled off and the residue is chromatographed on silica gel with chloroform. The 4-[(5-isopropoxy-2-pentenylthio)-methyl]-chlorobenzol is obtained as colourless oil having a B.P. of 110°-112°/5.10-4 mm. nD20 = 1.5391.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03978134
Source datasetuspto-grants-1976_08
ORD IDord-cdcb5d8ad3064f5f9509504b411f788b
Source noteuspto-grants-1976_08