HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 4515Generated: October 26, 2026
Phosgene → 4-(5-Bromo-2-pyrimidinyloxy)-3-chlorophenylisocyanate
https://huagongshe.com/reaction/4515
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosgene | HCID 6371 | — |
| Reactant | 4-(5-Bromo-2-pyrimidinyloxy)-3-chloroaniline | HCID 13771440 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-(5-Bromo-2-pyrimidinyloxy)-3-chlorophenylisocyanate | HCID 10245850 | 95.1% |
Reaction Steps
Into a flask, a solution of 0.02 mol of phosgene in 30 ml of ethyl acetate was introduced. To this solution, a solution of 3 g of 4-(5-bromo-2-pyrimidinyloxy)-3-chloroaniline in 10 ml of ethyl acetate was dropwise added at room temperature. The mixture was reacted at room temperature for 3 hours under stirring and further under reflux for one hour. After completion of the reaction, ethyl acetate was distilled off under reduced pressure, and the residue was vacuum-dried to obtain 3.10 g of 4-(5-bromo-2-pyrimidinyloxy)-3-chlorophenylisocyanate having a melting point of from 63 to 68° C. (2) Into a flask, 1.22 g of 4-(5-bromo-2-pyrimidinyloxy)-3-chlorophenylisocyanate obtained in the above step was introduced, and 20 ml of toluene was added thereto. Further, 0.62 g of 2-nitrobenzamide was added under stirring. The mixture was reacted under reflux for 4 hours. After completion of the reaction, 5 ml of methanol was added to the reaction product, and the mixture was cooled. The precipitated crystals were collected by filtration to obtain 0.79 g of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04727077 |
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| Source dataset | uspto-grants-1988_02 |
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| ORD ID | ord-7ff718f3b7e94c629eff1d63f4573f1b |
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| Source note | uspto-grants-1988_02 |
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