HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649909Generated: October 31, 2026
Morpholine → benzyl 2(S)-morpholinocarbonyloxy-3-phenylpropionate
https://huagongshe.com/reaction/1649909
Participants
| Role | Name | HCID | Charge |
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| Reactant | Morpholine | HCID 8083 | — |
| Reactant | Diphosgene | HCID 10426 | — |
| Reactant | Benzyl (S)-(-)-2-hydroxy-3-phenylpropionate | HCID 10377698 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | benzyl 2(S)-morpholinocarbonyloxy-3-phenylpropionate | HCID 18638974 | — |
Reaction Steps
To a solution of benzyl 2(S)-hydroxy-3-phenylpropionate (256 mg) in dry tetrahydrofuran (10 ml) was added trichloromethyl chloroformate (0.122 ml). The mixture was refluxed for 18 hours. The mixture was cooled to 0° C., and morpholine (348 mg) was added thereto. The mixture was stirred at the same temperature for 3 hours. After evaporation of the solvent, the residue was dissolved in ethyl acetate (40 ml). The solution was washed with 5% hydrochloric acid, 1M sodium bicarbonate solution and water successively, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified with silica gel column chromatography (25% ethyl acetate in n-hexane as eluent) to give benzyl 2(S)-morpholinocarbonyloxy-3-phenylpropionate (367 mg) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04921855 |
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| Source dataset | uspto-grants-1990_05 |
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| ORD ID | ord-26fe57fbb21e4e4195064ef4889b88cb |
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| Source note | uspto-grants-1990_05 |
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