HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 549137Generated: October 29, 2026
Water → (2R)-3-(benzyloxy)-2-(tritylamino)propan-1-ol
https://huagongshe.com/reaction/549137
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | methyl O-benzyl-N-trityl-L-serinate | HCID 67156483 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (2R)-3-(benzyloxy)-2-(tritylamino)propan-1-ol | HCID 67156691 | 100.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07943609B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-0d3dcd6697b5453fa7c8b83b97677612 |
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| Source note | uspto-grants-2011_05 |
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