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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1277835Generated: October 31, 2026

Pyridine → HCID 54495907, compound

https://huagongshe.com/reaction/1277835

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantEthyl chloroformateHCID 10928—
ReactantHCID 23451844HCID 23451844—
ProductHCID 54495907HCID 54495907—
ProductHCID 57214149HCID 57214149—

Reaction Conditions

Temperature5 °C

Reaction Steps

[4-(3-Pentylphenoxy)-3-pentylphenyl]benzenamine (0.1 mole) and pyridine (50 ml) are charged into a glass reaction vessel fitted with a mechanical stirrer and thermometer and are cooled to about 5° C. Ethyl chloroformate (0.125 mole) is added, with stirring, at about 5° C. Stirring is continued for a period of about 30 minutes at about 5° C., then for an additional 16 hours at room temperature. The mixture is then washed with 2 portions of water (50 ml), dried and the solvent is then removed to yield the desired product ethyl [4-(3-pentylphenoxy)-3-pentylphenyl]carbamate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04279637
Source datasetuspto-grants-1981_07
ORD IDord-62051c47a52441c5beeaf9cc33133d66
Source noteuspto-grants-1981_07