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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066739Generated: October 29, 2026

1,1-Dichloroethane → HCID 14581394, compound

https://huagongshe.com/reaction/1066739

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1-DichloroethaneHCID 6365—
ReactantVinyl chloroformateHCID 78808—
Reactant4-(4-Methyl-1-piperazinyl)-2,1,3-benzothiadiazoleHCID 14581393—
ProductHCID 14581394HCID 14581394—

Reaction Steps

To a 25 ml round-bottomed flask equipped with condenser and nitrogen inlet were added 620 mg (2.64 mmol) of 4-(2,1,3-benzothiadiazolyl)-N-methylpiperazine, 0.224 ml (2.64 mmol) vinyl chloroformate, and 15 ml dichloroethane. The reaction was refluxed 16 hours, cooled, and evaporated. The residue was chromatographed on silica gel using methylene chloride/ethyl acetate as eluent, and the product fractions collected to give yellow solid 4-(2,1,3-benzothiadiazolyl)-N-vinyloxycarbonylpiperazine, 530 mg (69%). NMR (d, CDCl3): 3.6 (m, 4H), 3.8 (m, 4H). 4.4-5.0 (m, 2H), 6.6-7.6 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06245766B1
Source datasetuspto-grants-2001_06
ORD IDord-ccb478f9383142358e655387b262b353
Source noteuspto-grants-2001_06