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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1241496Generated: October 31, 2026

Oxalyl chloride → HCID 178445652, compound

https://huagongshe.com/reaction/1241496

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 178445657HCID 178445657—
SolventDichloromethaneHCID 6344—
ProductHCID 178445652HCID 178445652—

Reaction Steps

2.0 g (10.85 mmol) cis-4-tert-Butylcyclohexanecarboxylic acid (Example 42A) are dissolved in 50 ml dichloromethane, 1.65 g (13.02 mmol) ethanedioyl dichloride are added and the solution is stirred at room temperature for one hour. The mixture is then stirred at reflux for two hours and, after cooling down to room temperature, evaporated to dryness in vacuo. The residue is then dissolved in toluene two times and again evaporated to dryness in vacuo. The residue is used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115602B2
Source datasetuspto-grants-2006_10
ORD IDord-64d0a7edfd84440e91a2998bec707f31
Source noteuspto-grants-2006_10