Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methane | HCID 297 | — |
| Reactant | HCID 86584392 | HCID 86584392 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 70232632 | HCID 70232632 | 99.9% |
Reaction Steps
34.8 g (0.075 mole) of 1,3-bis (4-nitrophenoxy)-2-propyl cinnamate, 15 g of carbon black containing 5% Pt and 2% iron (product with water content of approximately 50%), and 300 ml of 1,4-dioxane were placed in a reaction vessel (hydrogenating apparatus). And stirring was conducted by heating at 60° C. under a hydrogen atmosphere. In approximately 8 hours, 10.8 L of hydrogen was absorbed and the reaction was completed when the absorption of hydrogen stopped. Then the reacted solution was separated by filtration for removing the catalyst and the filtrate was concentrated. 30.3 g of 1,3-bis (4-aminophenoxy)-2-propyl cinnamate was yielded. The exothermic peak temperature was 230° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06689899B2 |
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| Source dataset | uspto-grants-2004_02 |
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| ORD ID | ord-5ade9ebbcc484fcaa583b8b0ec05586e |
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| Source note | uspto-grants-2004_02 |
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