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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2115674Generated: October 30, 2026

Sodium borohydride → 1-Tert-butyl 3-methyl 4-hydroxypiperidine-1,3-dicarboxylate

https://huagongshe.com/reaction/2115674

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant1-tert-Butyl 3-methyl 4-oxopiperidine-1,3-dicarboxylateHCID 11276893—
SolventMethanolHCID 887—
Product1-Tert-butyl 3-methyl 4-hydroxypiperidine-1,3-dicarboxylateHCID 1853480690%

Reaction Steps

To a cold (0° C.) solution of 1-tert-butyl 3-methyl 4-oxo-1,3-piperidinedicarboxylate (134.0 g, 520.8 mmol) in methanol (800 mL) was added NaBH4 (9.85 g, 260.4 mmol) portionwise. The resulting mixture was stirred overnight to be allowed to warm to room temperature. The solvent was removed under reduced pressure, the residue was dissolved into ethyl acetate, washed with brine, dried over MgSO4, filterd, and concentrated under reduced pressure to give 1-tert-butyl 3-methyl 4-hydroxy-1,3-piperidinedicarboxylate, which was used for the next reaction without further purification. (120.8 g, yield 90%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07435743B2
Source datasetuspto-grants-2008_10
ORD IDord-8bda5a9c62c14c4db63c59660261a931
Source noteuspto-grants-2008_10