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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1611151Generated: October 30, 2026

1-Tert-butyl 3-methyl 1,2,5,6-tetrahydropyridine-1,3-dicarboxylate → HCID 22258851, compound

https://huagongshe.com/reaction/1611151

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Tert-butyl 3-methyl 1,2,5,6-tetrahydropyridine-1,3-dicarboxylateHCID 11128444—
ReactantDiisobutylaluminumhydrideHCID 21225700—
SolventTolueneHCID 1140—
ProductHCID 22258851HCID 2225885194%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cold (−20° C.) solution of 1-tert-butyl 3-methyl 5,6-dihydro-1,3(2H)-pyridinedicarboxylate (700.0 mg, 2.90 mmol) in dry toluene (40 mL) was added a solution of diisobutylaluminum hydride in toluene (1.5M, 4.83 mL, 7.25 mmol) dropwise under an argon atmosphere. The reaction mixture was stirred at 0° C. for 30 min and then stirred at room temperature. The reaction was quenched by an addition of water and the stirring was continued for additional 1 hr. The precipitated aluminum salts were filtered off. The filtrate was diluted with saturated NH4Cl solution, extracted with ethyl acetate. The separated organic phase was washed with brine, dried over MgSO4, filtered and evaporated to give tert-butyl 5-(hydroxymethyl)-3,6-dihydro-1(2H)-pyridinecarboxylate, which was used for the next reaction without further purification. (580.0 mg, yield 94%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06984649B1
Source datasetuspto-grants-2006_01
ORD IDord-39d5d463b6e44f7aa43d9cdb31adde62
Source noteuspto-grants-2006_01