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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2371867Generated: November 3, 2026

2-Methylthiazolidine → HCID 19905282, compound

https://huagongshe.com/reaction/2371867

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethylthiazolidineHCID 32196—
Reactant2-Chloro-4'-fluoropropiophenoneHCID 67672—
ReactantSodium AcetateHCID 517045—
SolventEthanolHCID 702—
ProductHCID 19905282HCID 1990528284.1%

Reaction Steps

3.73 g (0.02 mol) of β-chloro-4-fluoropropiophenone are added in little portions at room temperature to a suspension containing 2.06 g (0.02 mol) of 2-methylthiazolidine and 1.64 g (0.02 mol) of anhydrous sodium acetate in 20 ml of ethanol over 30 minutes under stirring. After stirring for an additional 3 hours, the reaction mixture is evaporated, saturated sodium hydrogen carbonate solution is added to the oily yellow residue and it is extracted twice with 30 ml of ether each. After drying and evaporating the extract, the oily yellow residue is dissolved in acetone and acidified by 48% hydrobromic acid. Thus, 4.26 g of a white crystalline product are obtained and recrystallized twice from ethanol to give 2.00 g (29.9%) of hydrobromide of the title compound, m.p.: 151°-152° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05096902
Source datasetuspto-grants-1992_03
ORD IDord-cef2e62477e64803843e1171c57e1ad6
Source noteuspto-grants-1992_03