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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720032Generated: November 1, 2026

Ethyl chloroformate → HCID 22419897, compound

https://huagongshe.com/reaction/1720032

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
ReactantHCID 22419891HCID 22419891—
SolventPyridineHCID 1049—
ProductHCID 22419897HCID 2241989787.1%

Reaction Steps

To a stirred solution of 1,3-dihydro-6-fluoro-2,1-benzisothiazole-2,2-dioxide (2.57 g) in anhydrous pyridine (8 ml) was added ethyl chloroformate (1.79 g) at 0° C. under N2 atmosphere. The mixture was stirred for 30 minutes and concentrated in vacuo. Cold hydrochloric acid was added to the precipitate (pH=6). The resulting solution was extracted with ethyl acetate. The organic layer was washed with water and dried over magnesium sulfate. The crude product was purified by silica gel column chromatography (methylene chloride-ethyl acetate 95:5) to give 1-ethoxycarbonyl-1,3-dihydro-6-fluoro-2,1-benzisothiazole 2,2-dioxide (3.1 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05504095
Source datasetuspto-grants-1996_04
ORD IDord-2e5ae54318224027b47ac6bfe97c1c87
Source noteuspto-grants-1996_04