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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1263291Generated: October 31, 2026

Allyl bromide → HCID 53893713, compound

https://huagongshe.com/reaction/1263291

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
Reactant1-((Prop-1-en-1-yl)oxy)prop-1-eneHCID 138323—
ReactantHCID 13015711HCID 13015711—
SolventMethyl Ethyl KetoneHCID 6569—
SolventDiphenyl EtherHCID 7583—
SolventHexaneHCID 8058—
ProductHCID 53893713HCID 53893713—

Reaction Steps

A mixture of 2,3-dichloro-4-(2-fluorobenzoyl)phenol (98 g., 0.343 mole), K2CO3 (94 g., 0.68 mole), allyl bromide (37 ml., 0.425 ml.) and 750 ml. of 2-butanone was heated at reflux for 4 hours. After cooling the 2-butanone was partially evaporated and the residue distributed between methylene chloride and aqueous NaCl. The organic layer was dried and evaporated to give 105 g. of the intermediate propenyl ether as a liquid. This material was dissolved in an equal volume of diphenyl ether and heated at 250° for 3.5 hours. The cooled reaction mixture was diluted with hexane and washed several times with 1N aqueous KOH. The combined aqueous washes were acidified with 6N HCl and the resulting mixture extracted with methylene chloride. The methylene chloride solution was dried (MgSO4) and evaporated to a residue. Trituration with hexane gave 73 g. of solid product, m.p. 83°-84° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04456612
Source datasetuspto-grants-1984_06
ORD IDord-1097951a81314623a329d2e8d5f31fef
Source noteuspto-grants-1984_06