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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2237437Generated: October 30, 2026

1-Chloroethyl chloroformate → HCID 68468807, compound

https://huagongshe.com/reaction/2237437

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloroethyl chloroformateHCID 521305—
ReactantHCID 58256121HCID 58256121—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 68468807HCID 6846880754%

Reaction Conditions

Temperature22 °C

Reaction Steps

A solution of the product from step g) (727 mg, 2.33 mmol) in anhydrous dichloroethane (11.6 ml) was cooled to 0° C., treated with 1-Chloroethyl chloroformate (1.27 ml, 11.65 mmol) and the reaction was warmed to 22° C. for 1 hour. The reaction diluted with CH2Cl2 (50 ml) and washed with sat. NaHCO3 (25 ml). The sat. NaHCO3 was back extracted with CH2Cl2 and the combined organic layers were washed with brine (25 ml), dried (MgSO4) and concentrated providing an oily residue, which was taken up in anhydrous MeOH (75 ml) and refluxed for 1 hour. The MeOH was evaporated and the crude residue was triturated with ether and filtered providing 323 mg (54%) of the subtitle compound. 1H NMR (300 MHz, DMSO) δ 9.60 (br s, 2H); 3.14-3.28 (m, 6H); 2.97-3.50 (m, 2H); MS: ESI (positive): 222, 224 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07718647B2
Source datasetuspto-grants-2010_05
ORD IDord-47fed3f43d0c4826bf0d86082a9fe136
Source noteuspto-grants-2010_05