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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1833758Generated: October 31, 2026

Bromobenzene → Benzyl 3-Bromopropyl Ether

https://huagongshe.com/reaction/1833758

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromobenzeneHCID 7961—
Reactant3-Bromopropyl chloromethyl etherHCID 3799013—
ReactantMagnesiumHCID 5462224—
SolventDiethyl EtherHCID 3283—
ProductBenzyl 3-Bromopropyl EtherHCID 277606492%

Reaction Steps

To the Grignard reagent prepared from bromobenzene (46.3 g., 0.294 mole) and magnesium (7.15 g., 0.294 mole) in ether (150 ml.) is added, dropwise over one hour at 0°, a solution of 3-chloromethoxy-1-bromopropane (55.0 g., 0.294 mole) in ether (50 ml.). The resulting solution is stirred at 25° for 16 hours, then heated at reflux for 1/4 hour, cooled to 0° and cautiously treated with ice water (200 ml.) with vigorous stirring. After separating the phases, the aqueous layer is extracted with ether (200 ml.). The combined organic extract is washed with water, 5% potassium carbonate, water and saturated brine, dried over sodium sulfate and evaporated in vacuo leaving a pale yellow oil (64.4 g., 96%) which is distilled to provide the title compound as a colorless liquid (92% recovery), b.p. 140°-141°/14 mm.; pmr (CDCl3)δ2.12 (2H,p), 3.51 (2H,t), 3.60 (2H,t), 4.50 (2H,t) and 7.31 (5H,s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04066692
Source datasetuspto-grants-1978_01
ORD IDord-66f3cbf622624516942fef48de87a704
Source noteuspto-grants-1978_01