Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 5-Nitrobenzimidazole | HCID 7195 | — |
| Reactant | 1,1'-Biphenyl, mixt. with 1,1'-oxybis(benzene) | HCID 24670 | — |
| Reactant | Diethoxymethylenemalonate | HCID 23435867 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178470543 | HCID 178470543 | — |
Reaction Steps
An 82 g. portion (0.5 mole) of 5-nitrobenzimidazole in 1 L of ethanol is reduced over 5 g. of 5% palladium-charcoal catalyst containing 50% water. The reduction stops after a pressure drop of 97 psig. (97%) in 75 min. The catalyst is filtered, 108 g. (0.5 mole) of diethoxymethylenemalonate is added to the filtrate and the solution is boiled in an open flask until about one-half of the solvent has boiled away (ca. 2 hr.). The product sets to a solid cake upon cooling. Ethanol containing a little water is added to assist in breaking up the cake and the product is filtered, washed with cold ethanol-H2O (3:1) and air-dried; yield, 125 g. (83%). A 50 g. portion of this anil is added to 500 ml. of boiling Dowtherm over a 3-4 min. period and boiling is continued 4 min. longer. After cooling to room temperature the product is filtered, washed with Dowtherm, then benzene and air-dried; 44 g. of crude product is obtained. Extraction of this material with 500 ml. of boiling ethanol gives 22 g., m.p. 315°-316° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04716168 |
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| Source dataset | uspto-grants-1987_12 |
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| ORD ID | ord-560b8435c78d49978cbae6b6b886ee53 |
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| Source note | uspto-grants-1987_12 |
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