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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1080505Generated: October 25, 2026

Hydrochloric Acid → N-[1(S)-benzyl-3-hydroxy-2-oxopropyl]phthalimide

https://huagongshe.com/reaction/1080505

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium ChlorideHCID 5234—
Reactant(Vinyl-2-ylidenetris(oxy))tris(trimethylsilane)HCID 553067—
Reactant3-phenyl-2(S)-phthalimidopropionyl chlorideHCID 10567197—
Solvent1,4-DioxaneHCID 31275—
ProductN-[1(S)-benzyl-3-hydroxy-2-oxopropyl]phthalimideHCID 1026731978%

Reaction Conditions

Temperature95 °C

Reaction Steps

A mixture of 134 g of 3-phenyl-2(S)-phthalimido-propionyl chloride and 269.7 g of tris(trimethylsilyloxy)-ethylene was stirred at 95° C. for 5 hours. A further 54 g of tris(trimethylsilyloxy)ethylene were added and the mixture was stirred at 95° C. for a further 1.5 hours. The cooled reaction mixture was then treated with 435 ml of dioxan and 174 ml of 0.6N hydrochloric acid and the resulting mixture was heated to 85° C. for 30 minutes. The cooled mixture was saturated with sodium chloride and then extracted with diethyl ether. The ethereal solution was washed with aqueous sodium bicarbonate solution and evaporated. The resulting pale yellow solid was crystallized from ethyl acetate/n-hexane to give 103 g of N-[1(S)-benzyl-3-hydroxy-2-oxopropyl]phthalimide as a white solid, MS: m/e 310 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05580999
Source datasetuspto-grants-1996_12
ORD IDord-b79cc8c7dcdb49b29f92959c90a943f2
Source noteuspto-grants-1996_12