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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 717506Generated: October 31, 2026

2-Bromoethanol → (R)-2-(3-(Fluoromethyl)pyrrolidin-1-yl)ethanol

https://huagongshe.com/reaction/717506

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromoethanolHCID 10898—
ReactantPotassium CarbonateHCID 11430—
Reactant(R)-3-(Fluoromethyl)pyrrolidine hydrochlorideHCID 89619639—
SolventAcetonitrileHCID 6342—
Product(R)-2-(3-(Fluoromethyl)pyrrolidin-1-yl)ethanolHCID 8963451064.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of (R)-3-(fluoromethyl)pyrrolidine hydrochloride (Intermediate 8, 4.26 g, 30.6 mmol), 2-bromoethanol (4.35 mL, 61.3 mmol), and potassium carbonate (12.7 g, 92 mmol) in acetonitrile (120 mL) was heated at 80° C. overnight. After cooling, solids were filtered off and washed with acetonitrile. The filtrate was concentrated on a rotary evaporator to give a residue that was purified by silica gel chromatography eluting with 10:7 ethyl acetate/hexanes to 10:7:2:1 ethyl acetate/hexane/methanol/triethylamine to afford 2.9 g of (R)-2-(3-(fluoromethyl)pyrrolidin-1-yl)ethanol as a clear oil. 1H NMR (400 MHz, DMSO-d6) δ 4.44 (t, 1H), 4.34 (dd, 1H), 4.22 (dd, 1H), 3.44 (q, 2H), 2.58-2.51 (m, 1H), 2.48-2.38 (m, 5H), 2.32-2.28 (m, 1H), 1.85-1.74 (m, 1H), 1.39-1.31 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193714B2
Source datasetuspto-grants-2015_11
ORD IDord-77e6788e6a2044aeb4880d30a3814838
Source noteuspto-grants-2015_11