HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 463955Generated: October 26, 2026
Phenyl chloroformate → HCID 20185695, compound
https://huagongshe.com/reaction/463955
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenyl chloroformate | HCID 15891 | — |
| Reactant | 4-(Difluoromethoxy)-6-methylpyrimidin-2-amine | HCID 2817390 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 20185695 | HCID 20185695 | 58.6% |
Reaction Steps
3.9 g (0.025 mol) of phenyl chloroformate and 0.05 g of 4-dimethylamino-pyridine are added in succession to a solution of 9.0 g (0.05 mol) of 2-amino-4-difluoromethoxy-6-methyl-pyrimidine in 30 ml of absolute tetrahydrofuran. The solution is stirred at 20°-25° C. for 24 hours and the reaction mixture is then diluted with 250 ml of ethyl acetate and the precipitate is separated off. 3.1 g of 2-amino-4-difluoromethoxy-6-methyl-pyrimidine hydrochloride of melting point 204°-205° C. (decomposition) are thus obtained. To remove the residual starting material, the filtrate is eluted over a column containing the ion exchanger I® (MERCK), and the eluate is dried over sodium sulfate and evaporated. 4.0 g of 2-phenoxycarbonylamino-4-difluoromethoxy-6-methyl-pyrimidine are obtained as the crude product in the form of a viscous oil. After crystallisation, the product has a melting point of 56°-58° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04545811 |
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| Source dataset | uspto-grants-1985_10 |
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| ORD ID | ord-5611bf1ad9f14da098cb9937c123bff5 |
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| Source note | uspto-grants-1985_10 |
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