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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1910404Generated: October 30, 2026

Water → Tert-butyl 4-(hydroxymethyl)-4-(methoxymethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1910404

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiisobutylaluminumhydrideHCID 21225700—
Reactant1-Tert-butyl 4-ethyl 4-(methoxymethyl)piperidine-1,4-dicarboxylateHCID 66741448—
SolventTolueneHCID 1140—
ProductTert-butyl 4-(hydroxymethyl)-4-(methoxymethyl)piperidine-1-carboxylateHCID 6853315553.9%

Reaction Steps

To a solution of 1-tert-butyl 4-ethyl 4-(methoxymethyl)piperidine-1,4-dicarboxylate (2.05 g) in toluene (21 ml) was added 0.99 M solution of diisobutyl aluminum hydride in toluene (16.5 ml) under at 0° C. It was stirred at room temperature for 2 hours. Water was added and extracted with EtOAc. The organic phase was washed with water and brine, dried over MgSO4, evaporated off. The residue was purified by silica gel column to give tert-butyl 4-(hydroxymethyl)-4-(methoxymethyl)piperidine-1-carboxylate (0.95 g) as oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08603975B2
Source datasetuspto-grants-2013_12
ORD IDord-2797af7e864445298a079f5b512c8fbf
Source noteuspto-grants-2013_12