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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743879Generated: October 30, 2026

1-Chloroethyl chloroformate → HCID 10244387, compound

https://huagongshe.com/reaction/1743879

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloroethyl chloroformateHCID 521305—
ReactantHCID 10446058HCID 10446058—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 10244387HCID 1024438773.7%

Reaction Steps

To a solution of 8-chloro-3-methyl-2,3,4,5,10,11-hexahydro-1H,9H-cyclopenta[b][1,4]diazocino[7,8,1-hi]indole (1.0 g, 3.64 mmole) in dichloroethane (200 mL) was added 1-chloroethyl chloroformate (2.0 mL, 18.35 mmole) and refluxed for 24 hours. The reaction mixture was cooled to room temperature and the solvent removed in vacuo and replaced with methanol (200 mL) and refluxed for another 3 hours. The reaction mixture was 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 0.70 g of the title compound as a white solid. 0.12 g of the above solid was further treated with one equivalent of fumaric acid in ethanol to form a fumarate salt, mp 226-228° C. MS (ES) m/z 261.09 ([M+H]+), MS (ES) m/z 302.12 ([M+ACN+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07012089B2
Source datasetuspto-grants-2006_03
ORD IDord-dd5d7cdca86646b4967188703032fab8
Source noteuspto-grants-2006_03