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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2299903Generated: November 3, 2026

3-Methylbutanal → 4-[(4-Benzyloxy-phenyl)-(3-methyl-butyl)-amino]-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/2299903

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-MethylbutanalHCID 11552—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant4-(4-Benzyloxy-phenylamino)-piperidine-1-carboxylic acid tert-butyl esterHCID 10547949—
SolventDichloromethaneHCID 6344—
Product4-[(4-Benzyloxy-phenyl)-(3-methyl-butyl)-amino]-piperidine-1-carboxylic acid tert-butyl esterHCID 5371216885.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

4-(4-Benzyloxy-phenylamino)-piperidine-1-carboxylic acid tert-butyl ester (9.51 g, 24.9 mmol) was dissolved in CH2Cl2 (150 mL) and treated with isovaleraldehyde (2.7 mL, 24.9 mmol). The reaction was stirred for 30 minutes, then cooled to 0° C., treated with NaBH(OAc)3, allowed to warm to room temperature as the ice melted, and stir overnight. The reaction was diluted with CH2Cl2 (300 mL), washed twice with saturated sodium bicarbonate solution and once with brine, dried over Na2SO4, and concentrated. The crude material was chromatographed on silica gel eluting with 4% MeOH/CH2Cl2 to give 9.59 g (85%) of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06495715B2
Source datasetuspto-grants-2002_12
ORD IDord-6ed9fdc9f73a4842bfddc331b92c9e2e
Source noteuspto-grants-2002_12