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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1992665Generated: October 30, 2026

Iodoethane → Methyl (3S*,4R*)-4-(2,4-difluorophenyl)-1-ethylpyrrolidine-3-carboxylate

https://huagongshe.com/reaction/1992665

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantDiisopropylethylamineHCID 81531—
Reactantmethyl (3S,4R)-4-(2,4-difluorophenyl)pyrrolidine-3-carboxylateHCID 59130986—
SolventTetrahydrofuranHCID 8028—
ProductMethyl (3S*,4R*)-4-(2,4-difluorophenyl)-1-ethylpyrrolidine-3-carboxylateHCID 5913097968%

Reaction Steps

To a stirred solution of methyl (3S,4R)-4-(2,4-difluorophenyl)pyrrolidine-3-carboxylate, from preparation 19 (10.5 g, 43 mmol) in tetrahydrofuran (215 mL) at room temperature under dry nitrogen was added iodoethane (3.8 mL, 48 mmol) and N,N-diisopropylethylamine (8.3 mL, 48 mmol) in single portions. The resulting mixture was stirred at room temperature under dry nitrogen for 72 hours, then quenched by the addition of water (200 mL) and extracted with ethyl acetate (2×250 mL). The combined organic layers were dried (magnesium sulfate), filtered, and concentrated in vacuo. The residue was purified by flash column chromatography eluting with a 2:1 pentane:ethyl acetate mixture increasing polarity to 1:1. This afforded the title compound as a clear oil (7.9 g, 68%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07649002B2
Source datasetuspto-grants-2010_01
ORD IDord-8d8b71b26c6645308e3ac21c51cd9f83
Source noteuspto-grants-2010_01