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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1035542Generated: October 31, 2026

Water → (2R,3R)-3-(benzyloxy)-2-(tritylamino)butan-1-ol

https://huagongshe.com/reaction/1035542

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantAluminium lithium hydrideHCID 21226445—
Reactantmethyl O-benzyl-N-trityl-L-threoninateHCID 67156552—
SolventDiethyl EtherHCID 3283—
Product(2R,3R)-3-(benzyloxy)-2-(tritylamino)butan-1-olHCID 67157387100.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

Methyl O-benzyl-N-trityl-L-threoninate (4.61 g, 9.91 mmol) was dissolved in 100 mL of anhydrous Et2O and the solution was cooled to 0° C. under N2. Lithium aluminum hydride (2.28 g, 60 mmol) was added and the mixture was stirred for 2 hours. The reaction mixture was then sequentially treated with 2.28 mL of H2O, 2.28 mL of 15% NaOH solution and 6.84 mL of H2O. After stirring for 30 minutes, the reaction mixture was filtered to remove the white solid. The solid was washed with several portions of Et2O and the combined filtrates were concentrated under reduced pressure. Chromatography (SiO2, 10-20% ethyl acetate/hexanes) gave 4.34 g of (2R,3R)-3-(benzyloxy)-2-(tritylamino)butan-1-ol as a colorless syrup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546383B2
Source datasetuspto-grants-2013_10
ORD IDord-88ecb6470b1e4cb98fdde34f56637cb0
Source noteuspto-grants-2013_10