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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1193321Generated: October 28, 2026

4-Methoxybenzylamine → HCID 66799287, compound

https://huagongshe.com/reaction/1193321

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethoxybenzylamineHCID 75452—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactanttert-Butyl 3,3-dimethyl-4-oxopiperidine-1-carboxylateHCID 22278899—
SolventDichloromethaneHCID 6344—
ProductHCID 66799287HCID 6679928738%

Reaction Conditions

Temperature0 °C

Reaction Steps

tert-Butyl 3,3-dimethyl-4-oxopiperidine-1-carboxylate (3.3 g, 14.53 mmol, 1 eq) and 4-methoxybenzylamine (3.98 g, 29.07 mmol, 2 eq) were dissolved in dichloromethane (40 ml), and stirring was carried out for 2 h at RT. The reaction mixture was cooled to 0° C., and Na(OAc)3BH (9.24 g, 43.61 mmol, 3 eq) was added in portions. Then stirring was carried out for 16 h at RT. The reaction mixture was diluted with dichloromethane (150 ml), washed with water and sat. NaCl solution (in each case 100 ml), dried over sodium sulfate and concentrated under reduced pressure. The crude product was purified by column chromatography (Alox neutral, 10% ethyl acetate in hexane) (colourless oil). Yield: 38% (1.948 g, 5.59 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680159B2
Source datasetuspto-grants-2014_03
ORD IDord-fec72004c5f94bbca02947cd85f09a09
Source noteuspto-grants-2014_03