Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 10972868 | HCID 10972868 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 71014731 | HCID 71014731 | 92% |
Reaction Steps
Benzo[1,2-b;4,5-b′]dithiophene-4,4,8,8-tetracarboxylic acid tetraethyl ester (95 g) was suspended in dioxane (2850 g) and KOH (356 g) under inert atmosphere and heated to 50° C. Hydrogenperoxide (111 g; w=35%) was added in portions over 3.5 hours and the suspension heated at 50° C. for 20 hours. The reaction mixture was acidified with 2M HCl (3500 g) and the yellow precipitate filtered off, washed with water and dried in vacuum to yield benzo[1,2-b;4,5-b′]dithiophene-4,8-dicarboxylic acid (50.6 g) in 92% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09216994B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-d183b81b53f54132b7a26233271af9fa |
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| Source note | uspto-grants-2015_12 |
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