HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 8367Generated: October 25, 2026
1-Bromo-3-chloropropane → 2'-Methyl-4'-chloropropoxyacetophenone
https://huagongshe.com/reaction/8367
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromo-3-chloropropane | HCID 8006 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Hydroxy-2-methylacetophenone | HCID 70133 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2'-Methyl-4'-chloropropoxyacetophenone | HCID 69377079 | — |
Reaction Steps
A mixture of 4′-hydroxy-2′-methyl-acetophenone (10.5 g) and 1-bromo-3-chloropropane (7.6 mL) in acetone (70 mL) was treated with potassium carbonate (14.5 g). The mixture was stirred at 50° C. for approximately 18 hours. The reaction mixture was cooled to ambient temperature and partitioned between dichloromethane (200 mL) and water (200 mL). The aqueous layer was washed twice with fresh portions of dichloromethane (200 mL) and brine was used to break any emulsions. The organic fractions were combined, dried over sodium sulfate, and evaporated. The residue was re-dissolved in dichloromethane (100 mL) and washed with 0.5 M sodium hydroxide (100 mL) and brine (100 mL), dried over magnesium sulfate, filtered and evaporated to give the title compound which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07087757B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-d09efd5bbd8744ae90df923aa5ef3ad5 |
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| Source note | uspto-grants-2006_08 |
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