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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 271293Generated: October 26, 2026

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

https://huagongshe.com/reaction/271293

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 numberUS07452895B2
Source datasetuspto-grants-2008_11
ORD IDord-955178be882b404683e51d66c5fa93f9
Source noteuspto-grants-2008_11