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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066911Generated: November 1, 2026

Trifluoroacetic acid → (trans)-1-Benzyl-4-isobutyl-pyrrolidine-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1066911

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantBenzyl(methoxymethyl)((trimethylsilyl)methyl)amineHCID 353442—
ReactantEthyl 5-methylhex-2-enoateHCID 6436900—
SolventDichloromethaneHCID 6344—
Product(trans)-1-Benzyl-4-isobutyl-pyrrolidine-3-carboxylic acid ethyl esterHCID 6986159944.2%

Reaction Conditions

Temperature-5 °C

Reaction Steps

N-Benzyl-N-(methoxymethyl)trimethylsilylmethylamine (2.84 g, 12 mmol), followed by TFA (1.0 M solution in CH2Cl2, 1.0 mL, 1 mmol) were added to a solution of (E)-5-methyl-hex-2-enoic acid ethyl ester (1.56 g, 10.0 mmol) in methylene chloride (30 mL) maintained at −5° C. under nitrogen atmosphere. After 15 minutes, the bath was removed and stirring was continued overnight. Saturated sodium bicarbonate was added, and the organic portion was separated, washed with brine, and dried. The product was purified by chromatography on silica gel, and compound was eluted with 20% ethyl acetate in hexane to give (trans)-1-Benzyl-4-isobutyl-pyrrolidine-3-carboxylic acid ethyl ester 3 as an oil (1.28 g, 44%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06245801B1
Source datasetuspto-grants-2001_06
ORD IDord-264feddedee446da9f1f356b42220804
Source noteuspto-grants-2001_06