HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 392333Generated: October 29, 2026
Monobenzone → 3-[4-(Benzyloxy)phenoxy]-6-chloro-2-pyrazinecarbonitrile
https://huagongshe.com/reaction/392333
Participants
| Role | Name | HCID | Charge |
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| Reactant | Monobenzone | HCID 7638 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3,6-Dichloropyrazine-2-carbonitrile | HCID 22662845 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-[4-(Benzyloxy)phenoxy]-6-chloro-2-pyrazinecarbonitrile | HCID 22662788 | 79.1% |
Reaction Steps
In 25 mL of dimethylformamide was dissolved 2.5 g of 3,6-dichloro-2-pyrazinecarbonitrile. After adding 3.2 g of 4-(benzyloxy)phenol and 3.0 g of potassium carbonate, the mixture was stirred at room temperature for one hour. A mixture of 25 ml of ethyl acetate and 100 mL of water was added to the reaction mixture, and the organic layer was separated. The organic layer thus obtained was washed successively with water and saturated aqueous solution of sodium chloride and dried on anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. Diisopropyl ether was added to the residue, the insoluble matter was filtered off, and the filtrate was concentrated. The residue thus obtained was washed with n-hexane to obtain 3.84 g of 3-[(4-(benzyloxy)phenoxy)]-6-chloro-2-pyrazinecarbonitrile as a light brown-colored solid product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06800629B2 |
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| Source dataset | uspto-grants-2004_10 |
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| ORD ID | ord-6f1f6e73e2fc4e46b090e0eba055da6d |
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| Source note | uspto-grants-2004_10 |
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