Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | O-Toluidine | HCID 7242 | — |
| Reactant | HCID 22180099 | HCID 22180099 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 22180106 | HCID 22180106 | — |
Reaction Steps
The compound 1-adamantyl 4-carboxymethyl-2,3-difluoro-6-nitrophenyl carbonate is dissolved in excess ortho-toluidine. The reaction mixture is stirred at 200° C. for 6 hours. The mixture is allowed to cool and is dissolved in diethyl ether. The organic phase is washed with dilute aqueous hydrochloric acid, saturated aqueous sodium bicarbonate, and brine, is dried (MgSO4), and is concentrated in vacuo to afford the desired product. The product is purified by flash chromatography as necessary.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07030119B1 |
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| Source dataset | uspto-grants-2006_04 |
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| ORD ID | ord-aad06831eb2c4e4b97b913f05f429aa8 |
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| Source note | uspto-grants-2006_04 |
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