HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34281Generated: October 29, 2026
Sodium hydride → (2R,3R)-2,3-epoxybutyric acid N-tert.-butoxycarbonylmethyl-N-p-methoxybenzylamide
https://huagongshe.com/reaction/34281
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | tert-Butyl bromoacetate | HCID 79177 | — |
| Reactant | (2R,3R)-2,3-epoxybutyric acid p-methoxybenzylamide | HCID 13488847 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2R,3R)-2,3-epoxybutyric acid N-tert.-butoxycarbonylmethyl-N-p-methoxybenzylamide | HCID 86742306 | — |
Reaction Steps
A solution of 2.21 g of (2R,3R)-2,3-epoxybutyric acid p-methoxybenzylamide in 100 ml of THF is added dropwise to a mixture, stirred at 0° under an argon atmosphere, of 550 mg of sodium hydride dispersion (55-60% in oil) and 1.52 ml of bromoacetic acid tert.-butyl ester in 25 ml of THF. The reaction mixture is heated to room temperature and stirred for a further 1 hour (reaction monitored by thin-layer chromatography). Total reaction time: 90 minutes. The insoluble portions are filtered off and washed with THF and the combined filtrates are concentrated by evaporation. The resulting crude product is purified by chromatography over 150 g of silica gel (system: toluene, toluene/ethyl acetate 80:20). Concentration of the pure fractions by evaporation yields the amorphous title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04761408 |
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| Source dataset | uspto-grants-1988_08 |
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| ORD ID | ord-0d5f1f60881142b2aa9bebc35da62fdb |
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| Source note | uspto-grants-1988_08 |
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