HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1656878Generated: November 2, 2026
2-Chloroethylamine hydrochloride → HCID 19786224, compound
https://huagongshe.com/reaction/1656878
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Chloroethylamine hydrochloride | HCID 9793737 | — |
| Reactant | HCID 178527880 | HCID 178527880 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 19786224 | HCID 19786224 | 99.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05256362 |
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| Source dataset | uspto-grants-1993_10 |
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| ORD ID | ord-2ae5bd4769fb4233a2a1ca1592a61a59 |
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| Source note | uspto-grants-1993_10 |
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