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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 221569Generated: October 30, 2026

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

https://huagongshe.com/reaction/221569

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantAluminium lithium hydrideHCID 21226445—
Reactantmethyl O-benzyl-N-trityl-L-serinateHCID 67156483—
SolventDiethyl EtherHCID 3283—
Product(2R)-3-(benzyloxy)-2-(tritylamino)propan-1-olHCID 67156691100.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

Methyl O-benzyl-N-trityl-L-serinate (2.94 g, 6.52 mmol) was dissolved in 100 mL of anhydrous Et2O and the solution was cooled to 0° C. under N2. Lithium aluminum hydride (1.63 g, 42.9 mmol) was added and the mixture was stirred for 90 minutes. The reaction mixture was then sequentially treated with 1.63 mL of H2O, 1.63 mL of 15% NaOH solution and 4.90 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, 15-20% ethyl acetate/hexanes) gave 2.78 g of (2R)-3-(benzyloxy)-2-(tritylamino)propan-1-ol as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207162B2
Source datasetuspto-grants-2012_06
ORD IDord-a93f7366cfac42a7ba5ae2f28c6774b4
Source noteuspto-grants-2012_06