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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356698Generated: October 30, 2026

Benzyl Alcohol → benzyl chlorooxalate

https://huagongshe.com/reaction/356698

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantOxalyl chlorideHCID 65578—
Productbenzyl chlorooxalateHCID 1101985892.1%

Reaction Steps

In this example the product was prepared in two synthetic steps. In the first step benzyl alcohol was reacted with 50% molar excess of oxalyl chloride. Upon completion of the reaction the excess oxalyl chloride was stripped from the product at reduced pressure to produce benzyl chlorooxalate having an assay of 96.6% and in a corrected yield of 92.1%. In the second step benzyl chlorooxalate was reacted with 2,5-dimethyl-2,5-dihydroperoxyhexane, in the presence of pyridine, to yield the product as described below:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05837782
Source datasetuspto-grants-1998_11
ORD IDord-3b33bdba8e36490c84e99bd7a4585c12
Source noteuspto-grants-1998_11