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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1656878Generated: November 2, 2026

2-Chloroethylamine hydrochloride → HCID 19786224, compound

https://huagongshe.com/reaction/1656878

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloroethylamine hydrochlorideHCID 9793737—
ReactantHCID 178527880HCID 178527880—
SolventBenzeneHCID 241—
ProductHCID 19786224HCID 1978622499.7%

Reaction Conditions

Temperature80 °C

Reaction Steps

In 100 ml of benzene, 0.1 mol of 2-chloroethylamine hydrochloride and 0.1 mol of 2-mercaptothiazoline were dispersed, gradually heated to 80° C., and stirred for reaction at this temperature for 30 minutes. After completion of the reaction, the reaction mixture was filtered to obtain white 2-(2-aminoethylthio)-thiazoline dihydrochloride powder in a yield of 99.7%. In 100 ml of 36 wt % hydrochloric acid, 23.5 g (0.1 mol) of 2-(2-aminoethylthio)-thiazoline dihydrochloride was dissolved. The resultant solution was refluxed for 30 hours, to obtain cysteamine hydrochloride. Then, the cysteamine hydrochloride was concentrated to dryness under a vacuum and then thoroughly dissolved by heating to a temperature above 80° C. The solution was aspired with a Pasteur pipet 2 mm in mouth diameter and dropped onto a tetrafluoroethylene plate having the opposite side thereof cooled with water to 30° C. The white solid cysteamine hydrochloride heaps consequently deposited on the plate were hemispheres 3 to 5 mm in diameter and 2 to 3 mm in height.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05256362
Source datasetuspto-grants-1993_10
ORD IDord-2ae5bd4769fb4233a2a1ca1592a61a59
Source noteuspto-grants-1993_10