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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30287Generated: October 29, 2026

Oxalyl chloride → HCID 86229119, compound

https://huagongshe.com/reaction/30287

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 67206550HCID 67206550—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 86229119HCID 86229119—

Reaction Conditions

Temperature0 °C

Reaction Steps

The product from step c) (1064 mg, 3.53 mmol) was dissolved in 20 mL of dichloromethane and cooled to 0° C. under N2 atmosphere and oxalyl chloride (1345 mg, 10.59 mmol) was added, followed by 2 drops of DMF. The reaction was stirred at 0° C. for 15 minutes and was allowed to come to room temperature. The reaction mixture was stirred for 1.5 hours and was evaporated to dryness to give the subtitle compound as a solid. MS calculated for C17H18ClNOS+H: 320, observed as methyl ester [dissolved in methanol]+H: 316.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07423056B2
Source datasetuspto-grants-2008_09
ORD IDord-86e4200b507844be898358c1562c4fec
Source noteuspto-grants-2008_09