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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1602679Generated: November 1, 2026

Oxalyl chloride → HCID 19612334, compound

https://huagongshe.com/reaction/1602679

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant3-t-Butylperoxy-1,3-dimethylbutanolHCID 22065463—
ProductHCID 19612334HCID 1961233498.4%

Reaction Steps

In this example the product was prepared in two synthetic steps. In the first step 3-t-butylperoxy-1,3-dimethylbutanol was reacted with 100% molar excess of oxalyl chloride. Upon completion of the reaction the excess oxalyl chloride was stripped from the product at reduced pressure to produce 3-t-butylperoxy-1,3-dimethylbutyl chlorooxalate having an assay of 98.1% and in a corrected yield of 98.4%. In the second step 3-t-butylperoxy-1,3-dimethylbutyl chlorooxalate was reacted with 3-hydroperoxy-1,3-dimethylbutanol in the presence of pyridine to yield the product as described below:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05981787
Source datasetuspto-grants-1999_11
ORD IDord-ca21bbbc0a1d4da092d68e954c088b3d
Source noteuspto-grants-1999_11