Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2040435Generated: October 31, 2026

Phenyl chloroformate → HCID 67043797, compound

https://huagongshe.com/reaction/2040435

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyl chloroformateHCID 15891—
ReactantHCID 51037830HCID 51037830—
SolventPyridineHCID 1049—
ProductHCID 67043797HCID 6704379782.7%

Reaction Steps

Phenyl chloroformate (0.35 ml, 2.79 mmol) was added dropwise to a solution of Example 64 (300 mg, 0.624 mmol) in pyridine (6 ml) while cooling slightly. The reaction mixture was stirred at room temperature overnight. After addition of ice-water, the mixture was extracted with ethyl acetate, and the organic phase was washed several times with dilute citric acid solution and water. The organic phase was dried over magnesium sulfate and concentrated under reduced pressure. The residue was triturated with diethyl ether, and the resulting precipitate was filtered off, washed with diethyl ether and dried. 310 mg of the desired intermediate were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580842B2
Source datasetuspto-grants-2013_11
ORD IDord-d78cc28a9de04e1f9074bc2c0711029e
Source noteuspto-grants-2013_11