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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242568Generated: October 28, 2026

Water → Tert-butyl 4-(4-chlorophenyl)-4-hydroxymethylpiperidine-1-carboxylate

https://huagongshe.com/reaction/242568

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAluminium lithium hydrideHCID 21226445—
Reactant1-tert-Butyl 4-methyl 4-(4-chlorophenyl)piperidine-1,4-dicarboxylateHCID 49760245—
SolventDiethyl EtherHCID 3283—
ProductTert-butyl 4-(4-chlorophenyl)-4-hydroxymethylpiperidine-1-carboxylateHCID 5811768246%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a chilled solution of 4-(4-chloro-phenyl)-piperidine-1,4-dicarboxylic acid 1-tert-butyl ester 4-methyl ester (700 mg, 1.98 mmol) in 6 ml ether was added dropwise 2 ml lithium aluminium hydride 1M solution in ether. The reaction was stirred at 0° C. for 3 hours, then water (100 ml) was slowly added. The resulting gel was filtered and the aqueous filtrate was extracted three times with ether. The combined organic layers were dried with magnesium sulfate and concentrated under vacuum. Recovered oil was purified by silica gel chromatography, eluting with hexane-ethyl acetate (6:4) to give the title compound (297 mg, 46%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653096B2
Source datasetuspto-grants-2014_02
ORD IDord-ab29898024c048aaaff2ebde109fcceb
Source noteuspto-grants-2014_02