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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37120Generated: October 26, 2026

Dimethyl Sulfoxide → 6-cyano-3,4-dihydro-2,2-dimethyl-4(2-oxocyclopentyl)-2H-1,4-benzoxazine

https://huagongshe.com/reaction/37120

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
Reactant6-cyano-3,4-dihydro-2,2-dimethyl-4-(2-hydroxycyclopentan-1-yl)-2H-1,4-benzoxazineHCID 19934564—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventOxalyl chlorideHCID 65578—
Product6-cyano-3,4-dihydro-2,2-dimethyl-4(2-oxocyclopentyl)-2H-1,4-benzoxazineHCID 1068347452.2%

Reaction Steps

In 5 ml of methylene chloride was dissolved 0.2 ml of oxalyl chloride and at a constant temperature between -50° C. and -60° C., a solution prepared by dissolving 0.34 ml of dimethyl sulfoxide in 1 ml of methylene chloride was added dropwise. The mixture was stirred for 2 minutes, after which a solution of 0.54 g of 6-cyano-3,4-dihydro-2,2-dimethyl-4-(2-hydroxycyclopentan-1-yl)-2H-1,4-benzoxazine in 2 ml of methylene chloride was added dropwise. The mixture was further stirred for 15 minutes and 0.7 ml of triethylamine was added. The mixture was stirred for an additional 5 minutes, after which it was allowed to return to room temperature. The reaction mixture was diluted with 10 ml of water and extracted with methylene chloride. The extract was washed with aqueous sodium chloride solution and dried over anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure. The residue was recovered by filtration, washed with ethanol and recrystallized from ethyl acetate to give 0.28 g of 6-cyano-3,4-dihydro-2,2-dimethyl-4(2-oxocyclopentyl)-2H-1,4-benzoxazine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05420126
Source datasetuspto-grants-1995_05
ORD IDord-6ae0e0ccde2c4fd48a16193d6a52ab20
Source noteuspto-grants-1995_05