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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1439863Generated: October 25, 2026

Chloroacetyl chloride → (R)-4-chloroacetyl-2-(4-chlorophenyl)-3,4-dihydro-2H-1,4-benzothiazine

https://huagongshe.com/reaction/1439863

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantTriethylamineHCID 8471—
Reactant(R)-(+)-2-(4-chlorophenyl)-3,4-dihydro-2H-1,4-benzothiazineHCID 22847494—
SolventDichloromethaneHCID 6344—
Product(R)-4-chloroacetyl-2-(4-chlorophenyl)-3,4-dihydro-2H-1,4-benzothiazineHCID 53817053108.8%

Reaction Steps

To a suspension of (R)-(+)-2-(4-chlorophenyl)-3,4-dihydro-2H-1,4-benzothiazine (1.30 g, 0.005 mole) and triethylamine (1.66 ml, 0.012 mole) in dichloromethane (16 ml) is added dropwise a solution of chloroacetyl chloride (0.79 ml, 0.01 mole) in dichloromethane (4 ml) under ice cooling, and the mixture is stirred at room temperature for 45 minutes. After the solvent is distilled off, to the residue are added ethyl acetate and water, and the ethyl acetate layer is washed with aqueous sodium hydrogen carbonate solution, water and saline, dried over sodium sulfate and distilled to remove the solvent to give (R)-4-chloroacetyl-2-(4-chlorophenyl)-3,4-dihydro-2H-1,4-benzothiazine (1.84 g) as caramel.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05496815
Source datasetuspto-grants-1996_03
ORD IDord-aa0af4ba215d4de9a6f84d778db8bd01
Source noteuspto-grants-1996_03