HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 848948Generated: October 30, 2026
Potassium Iodide → HCID 54495420, compound
https://huagongshe.com/reaction/848948
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Bisphenol A | HCID 6623 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Butene, 1-bromo-3-methyl- | HCID 70092 | — |
| Solvent | Dimethyl Sulfide | HCID 1068 | — |
| Product | HCID 54495420 | HCID 54495420 | 80.7% |
Reaction Steps
After a 300-ml flask was charged with 17.9 g (0.12 mol) of 1-bromo-3-methyl-2-butene and 11.4 g (0.05 mol) of bisphenol A to dissolve them in 100 ml of DMS, 16.6 g (0.12 mol) of anhydrous potassium carbonate and 19.9 g (0.12 mol) of potassium iodide were added, and the mixture was stirred for 10 hours at 40° C. Thereafter, the reaction mixture was cooled, and salts formed were removed by filtration, and the filtrate was concentrated. The resultant crude product was dissolved in 100 ml of dichloromethane, and the solution was washed each 3 times with a 5% aqueous solution of potassium hydroxide and saturated saline and dried over magnesium sulfate. The solvent was then distilled off to obtain 14.7 g of bisphenol A bis(3-methyl-2-butenyl) ether [the formula (70)].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06010826 |
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| Source dataset | uspto-grants-2000_01 |
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| ORD ID | ord-bc43601d5f4b49d2b1da5bfa36536ddb |
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| Source note | uspto-grants-2000_01 |
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