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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186428Generated: November 1, 2026

Methanol → 4-(Hydroxymethyl)tetrahydro-2H-pyran-4-carbonitrile

https://huagongshe.com/reaction/1186428

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
ReactantMethyl 4-cyanooxane-4-carboxylateHCID 16726727—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product4-(Hydroxymethyl)tetrahydro-2H-pyran-4-carbonitrileHCID 2493699892%

Reaction Steps

Methyl 4-cyanotetrahydro-2H-pyran-4-carboxylate (2.93 g, 17.3 mmol) was dissolved in tetrahydrofuran (50 mL), methanol (10 mL) and water (5.0 mL). To this, sodium borohydride (1.31 g, 34.6 mmol) was added and the mixture was stirred at room temperature for 30 minutes. The reaction was stopped by addition of water to the reaction mixture, and extraction with ethyl acetate was performed, followed by washing with brine and drying over anhydrous sodium sulfate. The solvent was evaporated off under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate) to give 4-cyanotetrahydro-2H-pyran-4-ylmethanol (1.59 g, yield: 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673908B2
Source datasetuspto-grants-2014_03
ORD IDord-e0a4dcaf845e4ea990aabfca7bdeca90
Source noteuspto-grants-2014_03