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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2355523Generated: November 2, 2026

Triethylamine → Benzyl 5,6-dihydropyridine-1(2H)-carboxylate

https://huagongshe.com/reaction/2355523

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzyl chloroformateHCID 10387—
Reactant1,2,3,6-TetrahydropyridineHCID 12750—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductBenzyl 5,6-dihydropyridine-1(2H)-carboxylateHCID 1145861378%

Reaction Steps

A solution of 1,2,3,6-tetrahydropyridine (5.0 g, 60.15 mmol) and triethylamine (16.77 mL, 2 equiv) in CH2Cl2 (50 mL) was cooled to 0° C. (ice/water bath), Benzyl chloroformate (9.7 mL, 1.1 equiv) was added slowly. After 30 min, the reaction mixture was allowed to warm slowly to rt and stirred for 4 h. LC-MS showed the reaction was complete. The mixture was diluted with ether (300 mL), washed with 5% aq HCl (2×50 mL), satd aq NaHCO3 (40 mL) and brine (40 mL), and dried over Na2SO4. After concentration, benzyl 5,6-dihydropyridine-1(2H)-carboxylate (9.93 g, 78% yield) was left. LC-MS (3 min) tR=1.74 min., m/z 218 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07754737B2
Source datasetuspto-grants-2010_07
ORD IDord-d978655c71a0439d9e21d5eff3cc4152
Source noteuspto-grants-2010_07