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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1463000Generated: November 1, 2026

Bromochloromethane → Hexanedioic acid, chloromethyl phenylmethyl ester

https://huagongshe.com/reaction/1463000

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromochloromethaneHCID 6333—
ReactantBenzyl adipateHCID 19019622—
ProductHexanedioic acid, chloromethyl phenylmethyl esterHCID 1073182048%

Reaction Conditions

Temperature0 °C

Reaction Steps

To 350 ml of bromochloromethane cooled to 0° C. is added 67 g (0.14 mole) tetrabutylammonium salt of benzyl adipate half ester and the mixture is stirred overnight at 0° C. then allowed to warm to room temperature. The excess bromochloromethane is evaporated in vacuo, 400 ml ethyl ether is added to the residue and the mixture is stirred to form crystals of tetrabutylammonium bromide. The crystals are removed by filtration, washed with ether, stirred with ethyl acetate (300 ml) for one hour and refiltered and washed with ethyl acetate. The combined filtrates are evaporated in vacuo, the residue purified by chromatography on silica gel (1 kg), eluting with 2:1 hexane/ethyl acetate, to yield 19.1 g (48%) of the title compound. 1H--NMR (CDCl3) ppm (delta): 1.58-1.9 (m, 4H), 2.2-2.62 (m, 4H), 5.13 (s, 2H), 5.68 (s, 2H), 7.38 (s, 5H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04462934
Source datasetuspto-grants-1984_07
ORD IDord-151b26e5811e42e48182dd8c2746fdda
Source noteuspto-grants-1984_07