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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242595Generated: October 28, 2026

Water → 1-Tert-butoxycarbonyl-4-(4-chlorophenyl)-4-methoxypiperidine

https://huagongshe.com/reaction/242595

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactanttert-Butyl 4-(4-chlorophenyl)-4-hydroxypiperidine-1-carboxylateHCID 21997555—
SolventDimethylformamideHCID 6228—
Product1-Tert-butoxycarbonyl-4-(4-chlorophenyl)-4-methoxypiperidineHCID 2199757852%

Reaction Steps

4-(4-Chloro-phenyl)-4-hydroxy-piperidine-1-carboxylic acid tert-butyl ester (200 mg, 0.641 mmol) was added portionwise as a solid to a suspension of sodium hydride (0.018 g, 0.770 mmol) in dimethylformamide (6 mL) at room temperature. After 30 minutes, methyl iodide (0.109 g, 60 uL, 0.770 mmol) was added and the mixture was stirred overnight. The mixture was poured into an equal volume of water and extracted with ethyl acetate (2×10 mL). The ethyl acetate extracts were dried over magnesium sulfate, filtered, and concentrated in vacuo to give a tan oil. The crude oil was purified by silica gel chromatography (hexane to 60:40 hexane/ethyl acetate gradient) to afford 4-(4-Chloro-phenyl)-4-methoxy-piperidine-1-carboxylic acid tert-butyl ester as a clear oil (108 mg, 52%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653096B2
Source datasetuspto-grants-2014_02
ORD IDord-92b524db968f49efbaff75e4728f17c8
Source noteuspto-grants-2014_02