HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1623476Generated: November 1, 2026
Dicyclohexylcarbodiimide → HCID 23250757, compound
https://huagongshe.com/reaction/1623476
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 2-Iodoaniline | HCID 11995 | — |
| Reactant | 2-Butynoic acid | HCID 68535 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 23250757 | HCID 23250757 | 100% |
Reaction Steps
A mixture of 2-iodo-phenylamine (10 g, 45.7 mmol) and but-2-ynoic acid (4.6 g, 54.8 mmol) in dichloromethane (50 ml) was cooled to 0° C. Then 1,3-dicyclohexylcarbodiimide (14 g, 68.6 mmol) was added. After stirring for 3 hours at room temperature, the mixture was washed with water (20 ml). The organic layer was dried over sodium sulfate and concentrated to give the crude product but-2-ynoic acid (2-iodo-phenyl)-amide (13.0 g, 100%) as a yellow solid which was used in next step without purification. MS calcd. for C10H8INO 285.1, obsd. (ESI+) [(M+H)+] 286.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08778973B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-f65413ed659b478f9a80b19859da9e5f |
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| Source note | uspto-grants-2014_07 |
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