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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 467057Generated: October 30, 2026

Allyl bromide → HCID 20082700, compound

https://huagongshe.com/reaction/467057

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
Reactant1-(2-Bromoethyl)-4-chlorobenzeneHCID 23029—
ReactantMagnesiumHCID 5462224—
SolventDiethyl EtherHCID 3283—
ProductHCID 20082700HCID 2008270074.6%

Reaction Steps

To a flame-dried flask containing 7.75 g of magnesium turnings under ether was added 4-chlorophenethyl bromide (70 g) in anhydrous ether (250 mL) at such a rate as to maintain a gentle reflux. When the addition was complete, the mixture was heated under reflux for an additional hour and then treated dropwise over one hour with allyl bromide (27.6 mL, 38.6 g) in ether (75 mL) maintaining a gentle reflux. The resulting mixture was stirred overnight at room temperature and then poured onto 600 mL of ice-cold dilute sulfuric acid. The product was extracted with ethyl acetate and the combined extracts were washed with dilute aqueous potassium carbonate, dried (MgSO4) and evaporated. The resulting brown oil was distilled under reduced pressure to give 43 g of 5-(4-chlorophenyl)pent-1-ene, b.p. 74°-80° (2 mmHg) as a colorless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05158949
Source datasetuspto-grants-1992_10
ORD IDord-53c25b08e4374d8bb8095ade29bb032a
Source noteuspto-grants-1992_10