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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1594823Generated: October 27, 2026

Tetrahydrofuran → 2-Hydroxymethyl-tetrahydro-pyranol

https://huagongshe.com/reaction/1594823

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantEthyl tetrahydro-4-oxo-2H-pyran-2-carboxylateHCID 54067561—
Product2-Hydroxymethyl-tetrahydro-pyranolHCID 2170643161%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cooled (0° C.), stirred suspension of LiAlH4 (3.42 g, 90.0 mmol) in anhydrous THF (50 mL) was added dropwise a solution of 4-oxo-tetrahydro-pyran-2-carboxylic acid ethyl ester (5.17 g, 30.0 mmol). After stirring for 1 hour, the reaction was quenched by the slow, sequential addition of water (3.4 mL), 15% NaOH (3.4 mL), and water (10.0 mL). The inorganic salt was filtered off and extracted with EtOAc repeatedly since the product was absorbed on the solid. Solvent removal afforded 2.42 g (61%) of yellow oil. The crude mixture was carried to the next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06284764B1
Source datasetuspto-grants-2001_09
ORD IDord-45b7851e6e554fe494ac0c915fc2ef75
Source noteuspto-grants-2001_09