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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 749991Generated: October 30, 2026

Water → tert-butyl (2R)-2-(hydroxymethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/749991

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant(2R)-1-[(tert-butoxy)carbonyl]piperidine-2-carboxylic acidHCID 688618—
ReactantBorane;tetrahydrofuranHCID 2723981—
SolventTetrahydrofuranHCID 8028—
Producttert-butyl (2R)-2-(hydroxymethyl)piperidine-1-carboxylateHCID 693395399.1%

Reaction Conditions

Temperature2.5 °C

Reaction Steps

To a solution of (R)-Piperidine-1,2-dicarboxylic acid 1-tert-butyl ester (5 g, 21.8 mmol) in anhydrous THF (32 mL) at 0-5° C. was added borane-tetrahydrofuran complex (1M solution in THF) (3.6 g, 41.84 mmol) over a period of 15 min. The mixture was stirred at 0-5° C. for 2 h and then at rt for 2 h. The mixture was added over a period of 10 min to cold water (75 mL) and extracted with EtOAc (300 mL). The aqueous layer was re-extracted with EtOAc (2×150 mL). The organic layers were combined, dried over anhydrous Na2SO4 and concentrated to obtain the title product as a colorless oil (4.65 g., 99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07402684B2
Source datasetuspto-grants-2008_07
ORD IDord-b87738e6685748d0a0f579470ae564d5
Source noteuspto-grants-2008_07