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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1012240Generated: October 30, 2026

Sodium Hydroxide → tert-butyl (3R)-3-(hydroxymethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1012240

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantSodium SulfateHCID 24436—
Reactant1-tert-Butyl 3-ethyl (3R)-piperidine-1,3-dicarboxylateHCID 1514446—
ReactantAluminium lithium hydrideHCID 21226445—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Producttert-butyl (3R)-3-(hydroxymethyl)piperidine-1-carboxylateHCID 151444795%

Reaction Steps

To a suspension of lithium aluminum hydride (2.9.0 g, 76.3 mmol) in tetrahydrofuran (100 ml) was added a solution of 1-tert-butyl 3-ethyl (R)-piperidine-1,3-dicarboxylate (16.30 g, 63.6 mmol) in tetrahydrofuran (60 ml) over 20 min under ice-cooling, and the mixture was further stirred for 20 min. To the reaction mixture were successively added water (2.9 ml), 4N aqueous sodium hydroxide solution (2.9 ml), water (8.7 ml) and anhydrous sodium sulfate, and the mixture was stirred at room temperature for 1 hr. The reaction mixture was filtered, and the solvent was evaporated under reduced pressure to give tert-butyl (R)-3-hydroxymethylpiperidine-1-carboxylate (13.00 g, yield 95.0%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977331B1
Source datasetuspto-grants-2011_07
ORD IDord-1cb7fedc064a4927a69298f62326cc32
Source noteuspto-grants-2011_07