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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2059775Generated: October 25, 2026

4-Aminotetrahydro-2H-pyran-4-carboxylic acid hydrochloride → (4-Aminooxan-4-yl)methanol

https://huagongshe.com/reaction/2059775

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Aminotetrahydro-2H-pyran-4-carboxylic acid hydrochlorideHCID 2734400—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product(4-Aminooxan-4-yl)methanolHCID 18316484—

Reaction Steps

(4-Amino-tetrahydropyran-4-yl)-methanol is prepared by adding LAH (99%, 1.2 g), portionwise, to a stirred mixture of 4-aminotetrahydropyran-4-carboxylic acid hydrochloride (2.0 g, 11.0 mmol) in THF (30 mL) at 0° C. Upon completion of addition, the reaction mixture is warmed to room temperature and stirred for 1 hour. The reaction mixture is cooled to 0° C. and cautiously quenched by the portionwise addition of Na2SO4.10H2O (4 g). The reaction mixture is diluted with ethyl acetate, warmed to room temperature, and filtered through Celite to give the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08278314B2
Source datasetuspto-grants-2012_10
ORD IDord-81dc67934e4448a5b7b563d5fa75a2b6
Source noteuspto-grants-2012_10