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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1377533Generated: October 31, 2026

Allyl chloride → HCID 15860210, compound

https://huagongshe.com/reaction/1377533

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl chlorideHCID 7850—
ReactantHCID 15907399HCID 15907399—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventSodium HydroxideHCID 14798—
ProductHCID 15860210HCID 1586021065%

Reaction Steps

To a stirred solution of N-(3-cyclopentyloxy-4-methoxyphenylacetyl)-2-hydroxy-5-chloroaniline (78g, 0.21 mol) in ethanol (600 ml) and 1N NaOH in methanol (213 ml) was added allyl chloride (23.3 g, 0.31 mol). The mixture was heated under reflux for 8 hours, after which it was diluted with water and extracted twice with ethyl acetate. Evaporation of the ethyl acetate and crystallization of the residue from methanol gave 56.4 g (65%) of the title compound, mp 75°-76.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665737
Source datasetuspto-grants-1997_09
ORD IDord-560437e398eb426d8aa6f33a2e27fa52
Source noteuspto-grants-1997_09