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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 715725Generated: October 30, 2026

Benzyltrimethylammonium hydroxide → (R)-4-Acetyl-1-((S)-1-(4-methoxyphenyl)ethyl)pyrrolidin-2-one

https://huagongshe.com/reaction/715725

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyltrimethylammonium hydroxideHCID 66854—
Reactant4-Acetyl-1-[(1S)-1-(4-methoxyphenyl)ethyl]pyrrolidin-2-oneHCID 58072016—
Solvent1-ButanolHCID 263—
Product(R)-4-Acetyl-1-((S)-1-(4-methoxyphenyl)ethyl)pyrrolidin-2-oneHCID 58071853—

Reaction Conditions

Temperature25 °C

Reaction Steps

103 g of a mixture of diastereoisomers (R/S)-4-acetyl-1-[(S)-1-(4-methoxyphenyl)-ethyl]-pyrrolidine-2-one is dissolved in 155 mL 1-butanol at 25° C. 18 mL benzyltrimethylammonium hydroxide (40% solution in methanol) is added. The solution is stirred for 30 minutes at 25° C. The solution is cooled to 0° C. Precipitation starts. The suspension is stirred for 15 minutes at 0° C. 100 mL n-heptane is added slowly and the suspension is stirred for 30 minutes at 0° C. The addition of 100 mL portions of n-heptane is repeated 4 times with subsequent stirring of the suspension at 0° C. for 30 minutes. The precipitate is isolated, washed with n-heptane and dried at 50° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187478B2
Source datasetuspto-grants-2015_11
ORD IDord-ef2e10cc9990444da5ac7da4fd00888d
Source noteuspto-grants-2015_11