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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1437874Generated: November 1, 2026

Oxalyl chloride → HCID 57941380, compound

https://huagongshe.com/reaction/1437874

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant2-Oxobornane-3-carboxylic acidHCID 55250421—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 57941380HCID 5794138096%

Reaction Conditions

Temperature0 °C

Reaction Steps

Oxalyl chloride (2.8 mL, 32.1 mmol) was added over a period of 10 min to a solution of (1S,4S)-4,7,7-trimethyl-3-oxo-bicyclo[2.2.1]heptane-2-carboxylic acid (Intermediate 24; 2.1 g, 10.7 mmol) and N,N-dimethylformamide (3 drops) in dichloromethane (15 mL) at 0° C. The reaction mixture was stirred at 0° C. for 5 min and then at room temperature for 2 h. The solvent was evaporated, and the residue was co-evaporated three times with dichloromethane and then dried under high vacuum for 20 min to give (1S,4S)-4,7,7-trimethyl-3-oxo-bicyclo[2.2.1]heptane-2-carbonyl chloride (2.2 g, 96%) as an orange oil. This was used directly in subsequent steps without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622492B2
Source datasetuspto-grants-2009_11
ORD IDord-09d92524ddaf4166b2601d102433de23
Source noteuspto-grants-2009_11