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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1157008Generated: November 1, 2026

HCID 53755671, compound → 3-(4-Chlorobenzoyl)-2-methylbenzene hexanoic acid

https://huagongshe.com/reaction/1157008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 53755671HCID 53755671—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
SolventMethanolHCID 887—
Product3-(4-Chlorobenzoyl)-2-methylbenzene hexanoic acidHCID 20534489—

Reaction Steps

Hydrogen was passed through a mixture of 16.27 g of 6-[3'-(4-chlorobenzoyl)-2'-methyl-phenyl]-hex-4-enoic acid in 80 ml of methanol and 16.3 g of Raney nickel and then the catalyst was filtered off. The methoanol was distilled from the filtrate and the residue was taken up in methylene chloride. The solution was dried, treated with activated carbon, filtered and evaporated to dryness to obtain, after crystallization from a 1-1 isorpopyl ether-petroleum ether mixture, 11.15 g of 6-[3'-(4-chlorobenzoyl)-2'-methyl-phenyl]-hexanoic acid melting at 82° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04337353
Source datasetuspto-grants-1982_06
ORD IDord-077a4a3960cf4468a58083d413d2bbbf
Source noteuspto-grants-1982_06