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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1497323Generated: October 26, 2026

Phosphoric Acid → benzyl N-[(3S,4S)-4-hydroxytetrahydropyran-3-yl]carbamate

https://huagongshe.com/reaction/1497323

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphoric AcidHCID 1004—
ReactantNADP nicotinamide-adenine-dinucleotide phosphateHCID 5886—
ReactantSodium HydroxideHCID 14798—
Reactant(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanalHCID 107526—
ReactantMonobasic potassium phosphateHCID 516951—
Reactantbenzyl [(3S)-4-oxotetrahydro-2H-pyran-3-yl]carbamateHCID 60209900—
SolventWaterHCID 962—
Productbenzyl N-[(3S,4S)-4-hydroxytetrahydropyran-3-yl]carbamateHCID 60209901—

Reaction Conditions

Temperature105 °C

Reaction Steps

To a solution of potassium dihydrogen phosphate (62.7 g, 0.461 mol) in 3.6 L of water was added phosphoric acid to pH=7.0. To this solution was added glucose (112 g, 0.622 mol), NADP (3.6 g), GDH-103 (1.8 g), KRED 119 (3.6 g), and crude benzyl [(3S)-4-oxotetrahydro-2H-pyran-3-yl]carbamate (103.4 g, 0.4148 mol). After 17 h, the reaction was adjusted to pH=6.5 with 5 N NaOH. A white solid was collected via filtration and washed 2× with water (200 mL). The solid was suspended in 600 mL of toluene and stirred with an overhead stirrer at 105° C. for 1 h, then cooled to rt. A white solid was collected via filtration and washed with toluene (200 mL) to provide benzyl [(3S,4S)-4-hydroxytetrahydro-2H-pyran-3-yl]carbamate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09199939B2
Source datasetuspto-grants-2015_12
ORD IDord-8ca6ab4646c74c1b89a702d0f0c68a41
Source noteuspto-grants-2015_12