HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348224Generated: October 31, 2026
Hydrochloric Acid → HCID 22725850, compound
https://huagongshe.com/reaction/348224
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-tert-Butylphenol | HCID 7393 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 87695054 | HCID 87695054 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 22725850 | HCID 22725850 | 93% |
Reaction Steps
A mixture of 32.3 g (45 mmol) of N-(2,6-diisopropylphenyl)-1,6,9-tribromoperylene-3,4-dicarboximide (prepared in accordance with Example 1a of WO 96/22 332), 27.0 g (180 mmol) of p-tert-butylphenol, 16.6 g (120 mmol) of anhydrous, finely pulverized potassium carbonate and 1200 ml of N-methylpyrrolidone (NMP) was heated at 120° C. with stirring for 6 h. After cooling to room temperature, the reaction mixture was introduced with stirring into 4500 g of 6% strength by weight aqueous hydrochloric acid, the mixture was subsequently stirred for 2 h, and the precipitated solid was filtered off, washed to neutrality with water and dried under reduced pressure at 100° C. Filtration through a short silica gel column using methylene chloride as eluent, and removal of the solvent under reduced pressure, gave 38.9 g (93%) of the desired product in the form of reddish violet crystals having a softening point of 156° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07176255B2 |
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| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-45296fbcd7d1488792f8e293a89e5e23 |
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| Source note | uspto-grants-2007_02 |
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