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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1841855Generated: October 25, 2026

Pyridine → (1-Ethyl)cyclopentyl bromoacetate

https://huagongshe.com/reaction/1841855

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBromoacetyl bromideHCID 61147—
Reactant1-EthylcyclopropanolHCID 545093—
SolventDichloromethaneHCID 6344—
Product(1-Ethyl)cyclopentyl bromoacetateHCID 2267094484%

Reaction Steps

Pyridine (67.5 g, 0.854 mol) was added dropwise to a solution of ethylcyclopropanol (75.0 g, 675 mmol) in anhydrous dichloromethane (750 mL) under N2 at 0° C. and stirred for 5 minutes. Bromoacetyl bromide (172 g, 74.4 mL, 854 mmol) in dichloromethane (75 mL) was added dropwise and the solution stirred at 0° C. for 20 h. The pyridinium bromide was filtered off, washed with dichloromethane (2×300 mL) and the solid pyridinium bromide discarded. The combined organic layers were washed with water (4×750 mL), and concentrated in vacuo. The crude oil was purified via of silica gel flash column chromatography (neutralized with TEA, 1:0 to 99:1 heptane:ethyl acetate). After concentration, the oil was filtered to afford the title compound (130 g, 84%) as a light orange oil. NMR (500 MHz, (CD3)2SO) δ: 3.93 (s, 2H), 2.07-2.14 (m, 2H), 2.00 (q, J=7 Hz, 2H), 1.59-1.77 (m, 4H), 0.89 (t, J=7 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08945814B2
Source datasetuspto-grants-2015_02
ORD IDord-7604be3217b440c2bf8c45b20999617c
Source noteuspto-grants-2015_02