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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873931Generated: October 26, 2026

Oxalyl chloride → Benzyl 6-chloro-6-oxohexanoate

https://huagongshe.com/reaction/1873931

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantAdipic acid monobenzyl esterHCID 11075409—
SolventChloroformHCID 6212—
ProductBenzyl 6-chloro-6-oxohexanoateHCID 14788431—

Reaction Conditions

Temperature0 °C

Reaction Steps

Next, oxalyl chloride (52.2 g; 0.41 mol) was dissolved in CHCl3 (1000 ml), and cooled to 0° C. To this was slowly added a solution of 6(benzyloxy)-6-oxohexanoic acid, (81.0 g; 0.34 mol) in CHCl3 (250 ml), and stirring was continued for 18 hr at room temperature. The reaction mixture was concentrated, coevaporated with CHCl3 (2 times 250 ml), and dried in vacuo, to yield benzyl 6-chloro-6-oxohexanoate as a colourless liquid (87 g; 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304468B2
Source datasetuspto-grants-2012_11
ORD IDord-d2ec25a0c6af4a9daa70ebc1141b3185
Source noteuspto-grants-2012_11