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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 484334Generated: October 26, 2026

Triethylamine → 1-(4-nitrophenyloxycarbonyl)-1,2,5,6-tetrahydropyridine-3-carboxaldehyde-O-methyloxime

https://huagongshe.com/reaction/484334

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Nitrophenyl chloroformateHCID 82129—
Reactant1,2,5,6-Tetrahydropyridine-3-carboxaldehyde-O-methyloximeHCID 197313—
SolventDichloromethaneHCID 6344—
Product1-(4-nitrophenyloxycarbonyl)-1,2,5,6-tetrahydropyridine-3-carboxaldehyde-O-methyloximeHCID 307286395%

Reaction Steps

A solution of 97% 4-nitrophenyl chloroformate (1.5 g, 7.22 mmoles) in dichloromethane (15 mL) was added at 0° C. to a stirred solution of 1,2,5,6-tetrahydropyridine-3-carboxaldehyde-O-methyloxime (0.92 g, 6.6 mmoles) and triethylamine (0.92 mL, 6.6 mmoles) in dichloromethane (20 mL). The reaction mixture was then stirred at room temperature for 20 minutes, the solvent was evaporated and the residue was partitioned between water and ethyl acetate. The organic layer was dried (Na2SO4) and evaporated. The solid was recrystallized from benzene-cyclohexane to give 1.9 g (95%) of the desired product with mp 109°-110° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05231107
Source datasetuspto-grants-1993_07
ORD IDord-fd4c77fa32594158be7a2ba968f393e8
Source noteuspto-grants-1993_07