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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2398842Generated: October 25, 2026

Acetic Acid → HCID 178443035, compound

https://huagongshe.com/reaction/2398842

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant2,2,2-Trifluoroethylamine hydrochlorideHCID 9772—
ReactantSodium AcetateHCID 517045—
ReactantEthyl-m-[N,N-di(n-hexadecyl)aminomethyl]-thiobenzimidate DihydrochlorideHCID 12565115—
SolventChloroformHCID 6212—
ProductHCID 178443035HCID 17844303586%

Reaction Steps

Ethyl-m-[N,N-di(n-hexadecyl)aminomethyl]-thiobenzimidate dihydrochloride (1.074 g., 1.5 mmoles) was added to a slurry of 2,2,2-trifluoroethylamine hydrochloride (406 mg., 3.0 mmoles) and anhydrous sodium acetate (246 mmoles) in chloroform (10 ml.) and glacial acetic acid (0.3 ml., 5.3 mmoles). The mixture was held for 12 hours at room temperature. It was then diluted to 300 ml. with chloroform, washed with saturated aqueous sodium bicarbonate solution (2 × 50 ml.), washed with saturated aqueous sodium chloride solution (2 × 50 ml.), dried (Na2SO4) and filtered. The filtrate was acidified with a 10% solution of anhydrous hydrogen chloride in dioxane (5 ml.) and then evaporated in vacuo to a foam. The foam was crystallized from 1,2-dimethoxyethane [974 mg., 86% yield, Rf 0.39 (4:1, benzene:ethanol on silicic acid), m.p.-forms a gel at 125°-127° C⟧

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04025555
Source datasetuspto-grants-1977_05
ORD IDord-3c5f8f0d04f248a8a27e1d3f82b0ce62
Source noteuspto-grants-1977_05