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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 342356Generated: October 31, 2026

Oxalyl chloride → HCID 178439115, compound

https://huagongshe.com/reaction/342356

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantHCID 178439111HCID 178439111—
ReactantHCID 178443907HCID 178443907—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 178439115HCID 178439115—

Reaction Conditions

Temperature0 °C

Reaction Steps

After 27.6 g of the (2-(trans-4-(4-n-propylphenyl)cyclohexyl)ethyl)benzene obtained in (7) of Example 2 was dissolved in 200 ml of methylene chloride, it was cooled down to 0° C., and 24 g of aluminum chloride was added to the solution and stirred. Oxalyl chloride in an amount of 22.8 g was added dropwise little by little to the solution, and after the temperature of the solution was raised up to room temperature, it was stirred for 2 hours. After finishing of the reaction, it was added to 500 ml of water and extracted with 200 ml of methylene chloride. Organic layer was washed with water and dried over anhydrous magnesium sulfate, and the solvent was distilled off under a reduced pressure to obtain 20 g of 4-(2-(trans-4-(4-n-propylphenyl)cyclohexyl)ethyl)benzoyl chloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05858275
Source datasetuspto-grants-1999_01
ORD IDord-d28c547295e3482fa607c7c146d93aaa
Source noteuspto-grants-1999_01