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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1711416Generated: November 3, 2026

4-[3-(1-Naphthylsulfonylmethyl)-4-nitrophenoxymethyl]piperidine-1-carboxylic acid benzyl ester → 4-[4-Amino-3-(1-naphthylsulfonylmethyl)phenoxymethyl]piperidine-1-carboxylic acid benzyl ester

https://huagongshe.com/reaction/1711416

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-[3-(1-Naphthylsulfonylmethyl)-4-nitrophenoxymethyl]piperidine-1-carboxylic acid benzyl esterHCID 58828632—
SolventEthanolHCID 702—
Product4-[4-Amino-3-(1-naphthylsulfonylmethyl)phenoxymethyl]piperidine-1-carboxylic acid benzyl esterHCID 5882862485%

Reaction Steps

A mixture of 4-[3-(1-naphthylsulfonylmethyl)-4-nitrophenoxymethyl]-piperidine-1-carboxylic acid benzyl ester (0.9 g, 1.6 mmoles) and stannous chloride (1.8 g, 8 mmoles) in ethanol was heated at reflux temperature for 5 hours, cooled and concentrated under vacuum. The concentrate was diluted with water and extracted with EtOAc. The extracts were combined, dried over Na2SO4 and concentrated to afford the title compound (0.74 g, 1.36 mmoles).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790751B2
Source datasetuspto-grants-2010_09
ORD IDord-a346c6d0801a427a8c86f14cd9bcccbc
Source noteuspto-grants-2010_09