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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1354572Generated: October 31, 2026

Oxalyl chloride → HCID 11424769, compound

https://huagongshe.com/reaction/1354572

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 11229708HCID 11229708—
SolventDichloromethaneHCID 6344—
ProductHCID 11424769HCID 11424769112.8%

Reaction Steps

To a solution of 1-methyl-5-oxo-6,7,8,9-tetrahydro-5H-benzocycloheptene-7-carboxylic acid (5 g, 22.91 mmol) in dry dichloromethane (DCM) (15 mL), oxalyl chloride (6 mL, 68.75 mmol) was added dropwise at 0° C. The reaction mixture was stirred overnight at room temperature, concentrated in vacuo and to the residue dissolved in DCM (30 mL), methanol (15 mL) was added at 0° C. After stirring 1.5 h at room temperature, the mixture was diluted with water (60 mL) and extracted with DCM (100 mL), the organic layer was dried over Na2SO4, filtered and concentrated in vacuo to give 6.0 g of a yellow oil. Purification by flash chromatography on silica gel (hexane/diethyl ether: 8/2) afforded the title compound as a pale yellow oil (5.6 g, 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07223867B2
Source datasetuspto-grants-2007_05
ORD IDord-dafe0e9d668045258f4adb3ee86ec2e8
Source noteuspto-grants-2007_05