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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1799528Generated: October 31, 2026

Allyl bromide → 1-Allyl-4-fluorobenzene

https://huagongshe.com/reaction/1799528

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantHCID 178418676HCID 178418676—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
SolventAmmonium ChlorideHCID 25517—
Product1-Allyl-4-fluorobenzeneHCID 11147749—

Reaction Steps

Allyl bromide (4.33 mL, 50 mmol) was added dropwise to a solution of 4-fluorophenyl magnesium bromide (50 mmol) in tetrahydrofuran (25 mL) and diethyl ether (25 mL). After 16 hours, the reaction suspension was diluted with diethyl ether (100 mL) and saturated aqueous ammonium chloride (50 mL). The layers were separated, and the organic layer was washed with water (25 mL) and brine (25 mL), dried over magnesium sulfate, filtered, and concentrated to afford 1-allyl-4-fluorobenzene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08344144B2
Source datasetuspto-grants-2013_01
ORD IDord-66100db13b5442d9a0ec20c7036bd7d3
Source noteuspto-grants-2013_01