HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266864Generated: November 1, 2026
Bromine → 2-Bromo-1-[1-(3,4-dichlorophenyl)cyclobutyl]ethan-1-one
https://huagongshe.com/reaction/266864
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromine | HCID 24408 | — |
| Reactant | 1-Acetyl-1-(3,4-dichlorophenyl)cyclobutane | HCID 13083139 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-Bromo-1-[1-(3,4-dichlorophenyl)cyclobutyl]ethan-1-one | HCID 21258472 | — |
Reaction Steps
A solution of bromine (18 ml) in chloroform (80 ml) was added dropwise at 10°-15° C. over 1.5 hours to a stirred solution of the above 1-[1-(3,4-dichlorophenyl)-cyclobutyl]ethanone (89.6 g) in a mixture of methanol (120 ml) and chloroform (20 ml). When the addition was complete, the mixture was stirred at ambient temperature for 1 hour, then poured onto an excess of ice-water. The aqueous layer was separated and the product extracted into dichloromethane (2×150 ml). The combined organic solutions were washed with saturated aqueous sodium hydrogen carbonate solution (2×200 ml) then with water, dried over calcium chloride and the solvent removed in vacuo to yield an oil. The oil was distilled to give 2-bromo-l-[1-(3,4-dichlorophenyl)-cyclobutyl]ethanone (88.31 g), b.p. 148°-154° C./0.66 mbar.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05652271 |
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| Source dataset | uspto-grants-1997_07 |
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| ORD ID | ord-8a7d85cdad364527ad469952f7984b55 |
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| Source note | uspto-grants-1997_07 |
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