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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 401626Generated: October 30, 2026

1-Chloroethyl chloroformate → HCID 59625895, compound

https://huagongshe.com/reaction/401626

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloroethyl chloroformateHCID 521305—
ReactantHCID 59625794HCID 59625794—
SolventDichloromethaneHCID 6344—
ProductHCID 59625895HCID 59625895125%

Reaction Steps

To a solution of compound 8b (3.4 g, 7.7 mmol) in CH2Cl2 was added 1-chloroethyl chloroformate (2.5 mL, 23.1 mmol) at 0° C. under a N2 atmosphere. The ice bath was removed and the reaction stirred for 2 h. The organic phase was concentrated under reduced pressure, and MeOH was added to the resultant residue. The reaction was refluxed for 2 h at which time the solvent was removed under reduced pressure. The residue was partitioned between chloroform and aqueous HCl (1N). The aqueous layer was separated, made basic with aqueous NaOH (3N), and extracted with chloroform. The organic layer was then dried (K2CO3), filtered and concentrated to afford compound 8c (2.65 g). MS m/z (M+H+) 276.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741887B2
Source datasetuspto-grants-2014_06
ORD IDord-949b582f1923477182618361283b35bf
Source noteuspto-grants-2014_06