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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1869627Generated: November 2, 2026

Triethylamine → 1,1-Dimethylethyl 4-{[1-(cyclopropylmethyl)-4-piperidinyl]methyl}-1-piperidinecarboxylate

https://huagongshe.com/reaction/1869627

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant2-Cyclopropyl-2-hydroxyacetonitrileHCID 11389359—
Reactant4-Piperidin-4-ylmethyl-piperidine-1-carboxylic acid t-butyl esterHCID 49761197—
SolventDichloromethaneHCID 6344—
Product1,1-Dimethylethyl 4-{[1-(cyclopropylmethyl)-4-piperidinyl]methyl}-1-piperidinecarboxylateHCID 68885573—

Reaction Steps

1,1-Dimethylethyl 4-(4-piperidinylmethyl)-1-piperidinecarboxylate (may be prepared as described in Description 2) (2.0 g), cyclopropyl carboxaldehyde (1.6 ml) and triethylamine (1.99 ml) were stirred in dichloromethane (70 ml) at room temperature. After 10 min sodium triacetoxyborohydride (3.1 g) was added and the reaction was stirred at room temperature overnight. The reaction mixture was washed with saturated potassium carbonate solution (2×50 ml), saturated sodium hydrogen carbonate solution (2×50 ml) and saturated brine (50 ml). The organic phase was dried (MgSO4) and evaporated to give the title compound (D9) (2.0 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07638631B2
Source datasetuspto-grants-2009_12
ORD IDord-591176b5fb1349b58f029f4d5b668bc4
Source noteuspto-grants-2009_12