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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258389Generated: October 25, 2026

Methanol → 1-Benzyloxycarbonyl-3-hydroxymethyl-1,2,5,6-tetrahydropyridine

https://huagongshe.com/reaction/258389

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPotassium Sodium TartrateHCID 9357—
ReactantDiisobutylaluminum hydrideHCID 14487—
ReactantMethyl 1-benzyloxycarbonyl-1,2,5,6-tetrahydropyridine-3-carboxylateHCID 18797103—
SolventTetrahydrofuranHCID 8028—
Product1-Benzyloxycarbonyl-3-hydroxymethyl-1,2,5,6-tetrahydropyridineHCID 20089931—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of the compound of step 1 (2.0 g, 7.33 mmol) in tetrahydrofuran (30 ml) at -20° C. was added DIBAL-H. The mixture was warmed up to 0° C. and stirred at this temperature for 5 hours. Addition of methanol (5 ml) at 0° C. followed by addition of a saturated solution of Rochelle salt (10 ml) resulted in the formation of a white slurry. After stirring for an additional 2 hours, this was filtered; the filtrate was extracted with ether and the organic layer was washed with brine and dried over magnesium sulfate. Upon evaporation, the title compound was obtained as a slightly yellow oil (1.14 g, 4.6 mmol, 63% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05266569
Source datasetuspto-grants-1993_11
ORD IDord-1dd250861368497ab2e51083c1fb67ed
Source noteuspto-grants-1993_11