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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767335Generated: November 1, 2026

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

https://huagongshe.com/reaction/1767335

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 numberUS07232909B2
Source datasetuspto-grants-2007_06
ORD IDord-e3ce093e3f4e4a07a722cf56cd8075b8
Source noteuspto-grants-2007_06