HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 416025Generated: October 25, 2026
Potassium Carbonate → 5'-Chloro-2'-(2-methyl-2-propenyloxy)acetophenone
https://huagongshe.com/reaction/416025
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Chloro-6-hydroxyacetophenone | HCID 74061 | — |
| Reactant | 3-Bromo-2-methyl-1-propene | HCID 357785 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5'-Chloro-2'-(2-methyl-2-propenyloxy)acetophenone | HCID 58294038 | 97.9% |
Reaction Steps
A suspension of 5′-chloro-2′-hydroxyacetophenone (0.86 g, 5.0 mmol), potassium carbonate (1.4 g, 10 mmol) and 3-bromo-2-methylpropene (0.56 mL, 5.5 mmol) in anhydrous N,N-dimethylformamide (20 mL) was stirred at 60° C. for 4 hours. After cooling, the reaction mixture was diluted with water (100 mL), and the whole was extracted with ethyl acetate (100 mL). The organic layer was washed with saturated aqueous ammonium chloride solution (50 mL) and brine (50 mL) and dried over anhydrous magnesium sulfate. The solvent was removed in vacuo to give the title reference compound (1.1 g) as orange oil (Yield 96%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08088817B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-1609479122814f759c812f9af7a87ca2 |
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| Source note | uspto-grants-2012_01 |
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