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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 451518Generated: October 30, 2026

Allyl bromide → Methyl 2-(2-chloro-4-fluorophenyl)pent-4-enoate

https://huagongshe.com/reaction/451518

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
Reactant(2-Chloro-4-fluorophenyl)acetic acid methyl esterHCID 736123—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 2-(2-chloro-4-fluorophenyl)pent-4-enoateHCID 67342147—

Reaction Steps

To a chilled (−78° C.) solution of lithium hexamethydisilylazide (27.1 mL, 1 M in THF, 27.1 mmol) in THF (30 mL) was added methyl 2-(2-chloro-4-fluorophenyl)acetate (5 g, 24.7 mmol) in THF (10 mL). After stirring for 0.5 hour, allyl bromide (2.4 mL, 27.1 mmol) was added in a single portion, the cooling bath removed and the reaction allowed to warm to room temperature (0.5 hour). The reaction was diluted with ethyl acetate, washed with water, brine, and the organic phase was dried with sodium sulfate and the solvent was evaporated in vacuo. The residue was purified by column chromatography on silica gel using n-heptane/ethyl acetate (v/v 1:0 to 9:1) as eluent. The title compound was obtained as a colourless liquid (6.0 g, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08486967B2
Source datasetuspto-grants-2013_07
ORD IDord-4e326ceebe6c49219fba7618bae5416d
Source noteuspto-grants-2013_07