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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1870583Generated: October 30, 2026

Oxalyl chloride → HCID 53822961, compound

https://huagongshe.com/reaction/1870583

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 53990259HCID 53990259—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 53822961HCID 53822961—

Reaction Steps

To a 0° C. cold solution of 6.3 g of 3-[2-(tert-Butyl-dimethyl-silanyloxy)-phenyl]-acrylic acid tert-butyl-dimethyl-silyl ester and 8 drops of DMF in 15 ml of CH2Cl2 was added dropwise 2.0 ml of oxalyl chloride. After complete addition the reaction mixture was allowed to warm to room temperature and stirring was continued for 60 h. The reaction mixture was filtered, evaporated to dryness and taken up in MTBE. The solution was cooled in the refrigerator overnight, filtered and evaporated to yield 4.4 g of 3-[2-(tert-Butyl-dimethyl-silanyloxy)-phenyl]-acryloyl chloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06096918
Source datasetuspto-grants-2000_08
ORD IDord-daebd2009bed4fbc8175afccacd39185
Source noteuspto-grants-2000_08