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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337022Generated: October 28, 2026

Benzyl 4-formylpiperidine-1-carboxylate → 4-[(R)-[[(R)-(1,1-Dimethylethyl)sulfinyl]amino]phenylmethyl]-1-piperidinecarboxylic acid, phenylmethyl ester

https://huagongshe.com/reaction/337022

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl 4-formylpiperidine-1-carboxylateHCID 2776272—
Reactanttert-Butylsulfinamide, (R)-(+)-HCID 10964479—
CatalystCopper SulfateHCID 24462—
SolventDichloromethaneHCID 6344—
Product4-[(R)-[[(R)-(1,1-Dimethylethyl)sulfinyl]amino]phenylmethyl]-1-piperidinecarboxylic acid, phenylmethyl esterHCID 8666323374.9%

Reaction Steps

A mixture of 4-formyl-piperidine-1-carboxylic acid, benzyl ester (0.96 g), (R)-2-methyl-2-propanesulfinamide (0.51 g), anhydrous copper(II) sulphate (1.5 g) and dichloromethane (20 mL) was stirred at room temperature for 48 h. Copper(II) sulphate was filtered off and the filtrate concentrated. The residue was treated with dry dichloromethane (15 mL) and cooled to −78° C. A solution of phenylmagnesium bromide in diethyl ether (3M, 4 mL) was added dropwise. The mixture was slowly warmed to 0° C., then quenched with sat. aqueous NH4Cl solution. The mixture was stirred for 15 min and extracted into dichloromethane. The organic phase was dried (Na2SO4), filtered and concentrated in vacuo. The residue was purified (SiO2 chromatography eluting with iso-hexane:ethyl acetate (0-100%)) to give the title compound (623 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889692B2
Source datasetuspto-grants-2014_11
ORD IDord-1baf730eaab543d0934846a05a7b6416
Source noteuspto-grants-2014_11