Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 457119Generated: October 30, 2026

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

https://huagongshe.com/reaction/457119

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 numberUS07186729B2
Source datasetuspto-grants-2007_03
ORD IDord-bf717a8da08b4d6eb161840d31d2cc29
Source noteuspto-grants-2007_03