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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2309180Generated: October 26, 2026

Triethylamine → N-(phenoxycarbonylamino)-1,2,3,6-tetrahydropyridine

https://huagongshe.com/reaction/2309180

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPhenyl chloroformateHCID 15891—
Reactant1,2,3,6-Tetrahydropyridin-1-amine hydrochlorideHCID 19376047—
SolventDichloromethaneHCID 6344—
ProductN-(phenoxycarbonylamino)-1,2,3,6-tetrahydropyridineHCID 2015237692.1%

Reaction Conditions

Temperature5 °C

Reaction Steps

To a solution of N-amino-1,2,3,6-tetrahydropyridine hydrochloride (1.346 g) and triethylamine (2.024 g) in methylene chloride (60 ml) was added a solution of phenyl chloroformate (1.566 g) in methylene chloride (40 ml) and the mixture was stirred for 4 hours at 5° C. Evaporation of the solvent gave a residue, which was extracted with ethyl acetate (150 ml). The extract was washed with water and dried over magnesium sulfate. The solvent was evaporated in vacuo to give N-(phenoxycarbonylamino)-1,2,3,6-tetrahydropyridine (2.01 g), which was recrystallized from diisopropyl ether to give the desired compound (0.732 g) as colorless needles.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04694004
Source datasetuspto-grants-1987_09
ORD IDord-5a5455e251314c13b390d0213407f274
Source noteuspto-grants-1987_09