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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2071883Generated: October 30, 2026

Allyl chloride → Propane, 2-bromo-1-chloro-

https://huagongshe.com/reaction/2071883

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl chlorideHCID 7850—
Reactant1-Bromo-3-chloropropaneHCID 8006—
SolventCyclohexaneHCID 8078—
Product1-Bromo-3-chloropropaneHCID 8006—
ProductPropane, 2-bromo-1-chloro-HCID 181753%

Reaction Steps

The same process as in example 2 was carried out, but the cyclohexane was replaced by 3-bromo-1-chloropropane. The reaction developed in the same way. After 30 minutes of irradiation at 22° C, 90% of allyl chloride had been converted. The reaction product was degassed and the unreacted allyl chloride was distilled. The remaining product was formed by 3-bromo-1-chloropropane (solvent + formed product) and about 3% of 2-bromo-1-chloropropane. This operation has the advantage of making the solvent distillation unnecessary.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04049516
Source datasetuspto-grants-1977_09
ORD IDord-fd729aa701f2427aaa34fce67080442c
Source noteuspto-grants-1977_09