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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1193367Generated: October 31, 2026

Benzaldehyde → tert-Butyl 4-(benzyl(methyl)amino)piperidine-1-carboxylate

https://huagongshe.com/reaction/1193367

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactanttert-Butyl 4-(methylamino)piperidine-1-carboxylateHCID 15380702—
SolventDichloromethaneHCID 6344—
Producttert-Butyl 4-(benzyl(methyl)amino)piperidine-1-carboxylateHCID 2329200828%

Reaction Steps

tert-Butyl 4-(methylamino)piperidine-1-carboxylate (3.0 g, 14.019 mmol, 1.0 eq.) was dissolved in DCM (30 ml); benzaldehyde (1.7 ml, 16.823 mmol, 1.2 eq.) was added and the mixture was stirred for 1 hour at RT. NaBH(OAc)3 (4.81 g, 28.038 mmol, 3.0 eq.) was then added at 0° C. and the reaction mixture was stirred for 14 hours at RT. After monitoring by TLC, DCM (300 ml) was added to the reaction and washing was carried out in succession with sodium hydrogen carbonate solution (100 ml), water (100 ml) and sat. NaCl solution (100 ml). The organic phase was dried over sodium sulfate, concentrated under reduced pressure and purified by column chromatography (silica gel, 1% MeOH in DCM). Yield: 28% (1.2 g, 3.947 mmol)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680159B2
Source datasetuspto-grants-2014_03
ORD IDord-33583f16ce7c4a8ba482ca0ab770aa3c
Source noteuspto-grants-2014_03