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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 627074Generated: October 29, 2026

Cerium(III) chloride → tert-Butyl (3S,6S)-6-{[(tert-butyldimethylsilyl)oxy]methyl}-3-hydroxy-4-methyl-1,2,3,6-tetrahydropyridine-1-carboxylate

https://huagongshe.com/reaction/627074

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCerium(III) chlorideHCID 24636—
ReactantSodium borohydrideHCID 4311764—
Reactanttert-Butyl (6S)-6-{[(tert-butyldimethylsilyl)oxy]methyl}-4-methyl-3-oxo-1,2,3,6-tetrahydropyridine-1-carboxylateHCID 89852373—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventAmmonium ChlorideHCID 25517—
Producttert-Butyl (3S,6S)-6-{[(tert-butyldimethylsilyl)oxy]methyl}-3-hydroxy-4-methyl-1,2,3,6-tetrahydropyridine-1-carboxylateHCID 8985248691.3%

Reaction Steps

To a solution of cerium(III) chloride (14.68 g, 59.57 mmol) and (S)-tert-butyl 2-((tert-butyldimethylsilyloxy)methyl)-4-methyl-5-oxo-5,6-dihydropyridine-1(2H)-carboxylate (Intermediate 7, 21.18 g, 59.57 mmol) in methanol (300 mL) at 0° C. was added sodium borohydride (2.254 g, 59.57 mmol) portionwise. After 15 minutes, the reaction mixture was diluted with saturated ammonium chloride (100 mL) and water (100 mL), then extracted twice with diethyl ether. The organic extracts were washed with brine, dried over magnesium sulfate, filtered and concentrated. Silica gel chromatography (0%-20% ethyl acetate/hexanes) afforded the desired product (19.45 g, 91%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309245B2
Source datasetuspto-grants-2016_04
ORD IDord-f158ee2ca3cf4e13a2d995ca44fa243a
Source noteuspto-grants-2016_04