HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 990302Generated: November 1, 2026
Hydrochloric Acid → HCID 21894396, compound
https://huagongshe.com/reaction/990302
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 18421061 | HCID 18421061 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21894396 | HCID 21894396 | — |
Reaction Steps
A 4-necked 5-liter flask, equipped with a mechanical stirrer, a thermometer, and a condenser, is charged with methanol (800 g). Potassium hydroxide (440 g) is added in portions to the methanol solution. After the addition, the solution is cooled to 20° C. To this stirring solution, 1,1,1-tribromo-2,2-(4-hydroxyphenyl)ethane (420 g) is added in portions. The reaction temperature is kept below 40° C. After the addition, the temperature is raised to 50° C. and kept for 2 hours. The reaction mixture is cooled to room temperature and neutralized with 25% HCl solution. After the neutralization, the mixture is heated to reflux and water is added. The mixture is allowed to cool to the room temperature. The precipitates formed are filtered and dried to afford 1,1-dibromo-2,2-bis(4-hydroxyphenyl)ethene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06458993B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-455341ae15cc45159f0ff72b1f9c1931 |
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| Source note | uspto-grants-2002_10 |
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