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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 371717Generated: November 3, 2026

Thionyl Chloride → HCID 20355930, compound

https://huagongshe.com/reaction/371717

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantN-(2,2,3-Trichloro-1-hydroxypropyl)propanamideHCID 20355897—
ProductHCID 20355930HCID 20355930—

Reaction Steps

5.8 gm of N-(1-hydroxy-2,2,3-trichloropropyl)-propionamide were admixed with 20 ml of thionyl chloride, and the mixture was refluxed for 30 minutes. Subsequently, the reaction mixture was evaporated in vacuo. The crude N-(1,2,2,3-tetrachloro-n-propyl)-propionamide thus obtained was dissolved in 30 ml of tetrahydrofuran, and, while stirring, the solution was added to a solution of 1.75 gm of 1,2,4-triazole and 4.2 ml of triethylamine in 30 ml of tetrahydrofuran. After standing for 3 hours at room temperature, the reaction solution was admixed with water, and the tetrahydrofuran was distilled off in vacuo. A quickly solidifying oil was obtained, and the crystallizate was recrystallized from methanol/water. Yield: 4.6 gm; m.p. 167° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04087533
Source datasetuspto-grants-1978_05
ORD IDord-3148a63218264d029b87ac48a28591d7
Source noteuspto-grants-1978_05