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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743865Generated: November 2, 2026

1-Chloroethyl chloroformate → HCID 10220778, compound

https://huagongshe.com/reaction/1743865

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloroethyl chloroformateHCID 521305—
ReactantHCID 10378551HCID 10378551—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 10220778HCID 1022077830%

Reaction Steps

To a solution of 8-fluoro-3-methyl-2,3,4,5,9,10,11,12-octahydro-1H-[1,4]diazocino[7,8,1-jk]carbazole (0.37 g, 3.48 mmole) in dichloroethane (100 mL) was added 1-chloroethyl chloroformate (1.0 mL, 9.18 mmole) and the mixture refluxed for 24 hours. The reaction mixture was cooled to room temperature and the solvent removed in vacuo and replaced with methanol (100 mL) and refluxed for another 3 hours. The reaction mixture was then cooled to room temperature and the solvent removed in vacuo. The dark residue was dissolved in methylene chloride (200 mL) and washed with aqueous sodium hydroxide (1N, 150 mL), saturated sodium chloride (150 mL), dried (sodium sulfate) and concentrated. Purification by flash column chromatography (silica gel, 1.5% to 3% methanol in dichloromethane) provided 0.27 g of the title compound. 0.23 g of the above solid was further treated with one equivalent of fumaric acid in ethanol to form a fumarate salt, mp 177-179° C. MS (ESI) m/z 259 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07012089B2
Source datasetuspto-grants-2006_03
ORD IDord-7aeffecd51294974a3652f8cb8fa0a78
Source noteuspto-grants-2006_03