HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1513480Generated: October 28, 2026
Pyridine → Phenyl 4-carbamoylphenylcarbamate
https://huagongshe.com/reaction/1513480
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Pentane | HCID 8003 | — |
| Reactant | Phenyl chloroformate | HCID 15891 | — |
| Reactant | 4-Aminobenzamide | HCID 76079 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Phenyl 4-carbamoylphenylcarbamate | HCID 60631229 | 77% |
Reaction Steps
To a solution of 4-aminobenzamide (5.0 g, 36.7 mmol) and pyridine (2.9 g, 36.7 mmol)) in dry CH2Cl2 (100 mL) at −10° C., phenyl chloroformate (6.9 g, 44.1 mmol) was added dropwise, stirred at −10° C. for 30 min and then at room temperature for 30 minutes The reaction mixture was diluted with CH2Cl2 (100 mL) and washed with water (2×70 mL). The organic layer was dried over anhydrous Na2SO4 and concentrated to get the crude product. The crude product was dissolved in diethyl ether (15 mL) and sonicated for 10 minutes and then pentane (30 mL) was added, the resulting solid was filtered and washed with pentane to give phenyl 4-carbamoylphenylcarbamate (7.2 g, 77% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08217036B2 |
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| Source dataset | uspto-grants-2012_07 |
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| ORD ID | ord-1e3a6e16bf794ebca52e7f88f7005fb7 |
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| Source note | uspto-grants-2012_07 |
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