HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1456610Generated: October 31, 2026
Benzhydrylamine → Ethyl (2S,3S)-3-diphenylmethylcarbamoyloxirane-2-carboxylate
https://huagongshe.com/reaction/1456610
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzhydrylamine | HCID 7036 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | N-Hydroxysuccinimide | HCID 80170 | — |
| Reactant | (2S,3S)-3-(ethoxycarbonyl)oxirane-2-carboxylic acid | HCID 11030109 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ethyl (2S,3S)-3-diphenylmethylcarbamoyloxirane-2-carboxylate | HCID 57291692 | — |
Reaction Steps
To a solution of (2S,3S)-3-ethoxycarbonyloxirane-2-carboxylic acid (8.01 g, 50.0 mmol.) in ethyl acetate (120 mL) was added N-hydroxysuccinimide (5.76 g, 50.0 mmol.) and then added N,N'-dicyclohexylcarbodiimide (5.75 g, 50.0 mmol) under chilling with ice. The resulting mixture was stirred at 5° C. for one hour, and to the mixture was a solution of aminodiphenylmethane (9.17 g, 50.0 mmol.) in ethyl acetate (30 mL). The mixture was stirred at 5° C. for one hour and then at room temperature for one hour. The resulting N,N'-dicyclohexylurea (DC-Urea) was removed by filtration, and the filtrate was washed successively with 1N hydrochloric acid, an aqueous sodium hydrogen carbonate saturated solution, and an aqueous sodium chloride saturated solution, and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the residue was recrystalized from ethyl acetate--n-hexane, to give the desired compound as a white crystalline product (1.25 g, yield: 77%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05843992 |
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| Source dataset | uspto-grants-1998_12 |
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| ORD ID | ord-320293505c3847a19e7a6b4387c7b2cf |
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| Source note | uspto-grants-1998_12 |
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