HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 866113Generated: October 28, 2026
1,3-Dibromopropane → 1-[4-(3-Bromopropoxy)-3-methylmercaptophenyl]ethanone
https://huagongshe.com/reaction/866113
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,3-Dibromopropane | HCID 8001 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(4-Hydroxy-3-(methylthio)phenyl)ethan-1-one | HCID 3017662 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-[4-(3-Bromopropoxy)-3-methylmercaptophenyl]ethanone | HCID 10040638 | — |
Reaction Steps
A mixture of 1-[4-hydroxy-3-(methylmercapto)phenyl]-ethanone (5.4 g; 30 mmol), K2CO3 (4.2 g), 1,3-dibromopropane (8 g, 39 mmol) in acetonitrile (150 ml) was heated at reflux for 3 hours and stirred at room temperature overnight. Acetonitrile was removed at reduced pressure and the residue was extracted into dichloromethane (250 ml). Insolubles were filtered off. The dichloromethane solution was concentrated. The crude product was purified on a silica gel column (SiO2, 100 g; eluted with 3:2 hexane:dichloromethane, 1.6 l). The compound crystallized upon concentration, and the product (3.5 g, 39%) was recrystallized from ethanol (40 ml) to yield 1-[4-(3-bromopropoxy)-3-(methylmercapto)phenyl]ethanone as white needles, 2.0 g; m.p.=120°-122° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05569653 |
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| Source dataset | uspto-grants-1996_10 |
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| ORD ID | ord-900be93806f841718695fed111bc2a06 |
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| Source note | uspto-grants-1996_10 |
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