HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 977708Generated: October 28, 2026
1-Bromo-3-chloropropane → 1-[4-((3-Chloropropyl)thio]-3-methoxyphenyl]ethanone
https://huagongshe.com/reaction/977708
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Bromo-3-chloropropane | HCID 8006 | — |
| Reactant | Cyclohexane | HCID 8078 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(4-Thio-3-methoxyphenyl)ethanone | HCID 21960101 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1-[4-((3-Chloropropyl)thio]-3-methoxyphenyl]ethanone | HCID 10244271 | — |
Reaction Steps
A mixture of 1-(4-thio-3-methoxyphenyl)ethanone (10.0 g, 54.9 mmol), potassium carbonate (9.0 g, 65.1 mmol), and acetone (100 ml) was stirred at reflux under nitrogen for 30 minutes. The reaction was cooled to ambient temperature and a solution of 1-bromo-3-chloropropane (6.5 ml, 9.5 g, 60.4 mmol) dissolved in acetone (25 ml) was dripped into the reaction. After complete addition, the reaction was heated to reflux and stirred under nitrogen for 17 hours. After the reaction was carried to substantial completion, the reaction mixture was filtered and the resulting filter cake was washed with acetone. The filtrate was concentrated to provide an amber oil. A small sample was solidified by trituration with hot cyclohexane to provide 1-[4-[(3-chloropropyl)thio]-3-methoxyphenyl]ethanone as a yellow solid, 11.7 g, m.p.=53°-55° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05614543 |
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| Source dataset | uspto-grants-1997_03 |
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| ORD ID | ord-2c37971c21fa4acf8535fad61fab56c4 |
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| Source note | uspto-grants-1997_03 |
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