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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464735Generated: October 30, 2026

Hydrochloric Acid → HCID 23324906, compound

https://huagongshe.com/reaction/464735

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 54256950HCID 54256950—
ReactantHCID 54267983HCID 54267983—
SolventSodium HydroxideHCID 14798—
ProductHCID 23324906HCID 23324906—
ProductHCID 23324907HCID 23324907—

Reaction Steps

A solution of 93.4 g of 5-oxo-3-[4-(trifluoromethyl)phenyl]-2-pyrrolidinepropanoic acid methyl ester and 5-oxo-β-[4-(trifluoromethyl)phenyl]-2-pyrrolidinepropanoic acid methyl ester in 370 ml of 1 N aqueous sodium hydroxide solution is heated to 60° C. for four hours. Excess aqueous hydrochloric acid (1 N, 380 ml) is added and the solution concentrated under reduced pressure to give 5-oxo-β-[4-(trifluoromethyl)phenyl]-2-pyrrolidinepropanoic acid and 5-oxo-3-[4-(trifluoromethyl)phenyl]-2-pyrrolidinepropanoic acid. The acids are dissolved in 300 ml of acetic anhydride, and the solution is heated to 90° C. The solution is filtered hot and the filtrate concentrated in vacuo. The oil is chromatographed on silica gel (200-400 mesh) (elution with chloroform) to give cis-and trans-dihydro-1-(4-trifluoro-methylphenyl)-1H-pyrrolizine-3,5-(2H,6H)-diones as a white solid with a mp 173°-181° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04548947
Source datasetuspto-grants-1985_10
ORD IDord-10e5774165d341388e0c77af859721a5
Source noteuspto-grants-1985_10