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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242566Generated: October 28, 2026

Benzene → 1-tert-Butyl 4-methyl 4-(4-chlorophenyl)piperidine-1,4-dicarboxylate

https://huagongshe.com/reaction/242566

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantTrimethylsilyldiazomethaneHCID 167693—
Reactant1-(Tert-butoxycarbonyl)-4-(4-chlorophenyl)piperidine-4-carboxylic acidHCID 24828857—
SolventMethanolHCID 887—
Product1-tert-Butyl 4-methyl 4-(4-chlorophenyl)piperidine-1,4-dicarboxylateHCID 4976024588%

Reaction Steps

To a stirred 4-(4-chloro-phenyl)-piperidine-1,4-dicarboxylic acid mono-tert-butyl ester (852 mg, 2.5 mmol) in methanol (5 ml)-benzene (17.5 ml) was added 15 ml (trimethylsilyl)diazomethane (2.0 M solution in hexanes) at room temperature. The mixture was stirred for 16 hours at room temperature and concentrated in vacuo. The residual yellow oil was purified by silica gel chromatography eluting with hexane-ethyl acetate (9:1) to give the corresponding ester (780 mg, 88%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653096B2
Source datasetuspto-grants-2014_02
ORD IDord-b49858d3247c46d78f8051b5d5648e10
Source noteuspto-grants-2014_02