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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 852683Generated: October 31, 2026

Water → tert-Butyl 4-(2-hydroxyethyl)-4-(hydroxymethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/852683

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTert-butyl 1-oxo-2-oxa-8-azaspiro[4.5]decane-8-carboxylateHCID 10015228—
ReactantDiisobutylaluminumhydrideHCID 21225700—
SolventDichloromethaneHCID 6344—
Producttert-Butyl 4-(2-hydroxyethyl)-4-(hydroxymethyl)piperidine-1-carboxylateHCID 2195530463%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Diisobutylaluminium hydride (1.0M in dichloromethane, 3.60 mL, 3.60 mmol) was added over 10 minutes to a stirred, cooled (−78° C.) solution of 1,1-dimethylethyl 1-oxo-2-oxa-8-azaspiro[4.5]decane-8-carboxylate (Description 23, 400 mg, 1.57 mmol) in dichloromethane (4 mL) and the mixture stirred at −78° C. for 3 hours, then at 0° C. for 2 hours. Water (1.6 mL) was added very slowly at 0° C. and the mixture was warmed to room temperature and stirred overnight. The mixture was filtered through Hyflo™, washing with dichloromethane, and the solvent was evaporated under reduced pressure. The residue was purified by flash column chromatography on silica gel, eluting with ethyl acetate, to give the title compound (255 mg, 63%). m/z (ES+) 260 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253205B2
Source datasetuspto-grants-2007_08
ORD IDord-5974a0688a9943cb85161f12ac40f8e4
Source noteuspto-grants-2007_08