HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1951910Generated: November 3, 2026
Dicyclohexylcarbodiimide → HCID 58542422, compound
https://huagongshe.com/reaction/1951910
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 1-{[(Benzyloxy)carbonyl]amino}cyclopropane-1-carboxylic acid | HCID 3589012 | — |
| Reactant | (S)-methyl 2-(benzylamino)propanoate | HCID 10535780 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58542422 | HCID 58542422 | 71.2% |
Reaction Steps
N,N′-dicyclohexylcarbodiimide (6.0 g, 29.0 mmol) was added to a dichloromethane (150 ml) solution of methyl N-benzyl-L-alaninate (5.20 g, 26.9 mmol) and 1-{[(benzyloxy)carbonyl]amino}cyclopropanecarboxylic acid (6.30 g, 26.7 mmol) under ice cooling and the resulting mixture was stirred overnight at room temperature. The reaction mixture was concentrated under reduced pressure and then diluted with ethyl acetate, insoluble matter was removed by filtration and then the filtrate was washed with 1 N aqueous hydrochloric acid solution and saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure and the obtained residue was purified by silica gel column chromatography [n-hexane:ethyl acetate=1:3 (v/v)] to give the title compound (7.80 g, 71%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08404691B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-a20576f1588845bb921f80a3459610b8 |
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| Source note | uspto-grants-2013_03 |
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