HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 725120Generated: November 2, 2026
Dicyclohexylcarbodiimide → HCID 67694879, compound
https://huagongshe.com/reaction/725120
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | Acetamide, N-[4-(2-hydroxyethoxy)phenyl]- | HCID 170834 | — |
| Reactant | HCID 19711488 | HCID 19711488 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67694879 | HCID 67694879 | 55% |
Reaction Steps
0.57 g (2.75 mmol) of dicyclohexylcarbodiimide was portionwise added to a solution of 1.05 g (2.5 mmol) of 4-{N-[2,5-di(benzyloxy)benzoyl]amino}butyric acid (compound of Example 1) in 16 ml of anhydrous methylene chloride at room temperature under stirring. After stirring the solution at the same temperature for 10 minutes 0.54 g (2.75 mmol) of 2-[4-(acetylamino)phenoxy]ethanol and 0.03 g (0.25 mmol) of 4-(N,N-dimethyl-amino)pyridine were added. The reaction mixture was stirred at room temperature for 4 hours, then diluted with methylene chloride and the solid product was filtered. The filtrate was successively washed with 5% acetic acid, 5% sodium hydrogen carbonate solution and water, then dried and evaporated under reduced pressure. The residue was separated by chromatography on a silica gel column by eluating with a 95:5 mixture of chloroform and methanol to obtain 0.82 g (55%) of the aimed product, m.p.: 141°-143° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05705529 |
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| Source dataset | uspto-grants-1998_01 |
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| ORD ID | ord-c437e06d3f694fa18b631ecfb07d2cfb |
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| Source note | uspto-grants-1998_01 |
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