HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2228890Generated: October 30, 2026
Diethyl Ether → 8-Bromo-1-(4-chlorophenyl)octan-1-one
https://huagongshe.com/reaction/2228890
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Chlorobenzene | HCID 7964 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 8-bromooctanoyl Chloride | HCID 11402228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 8-Bromo-1-(4-chlorophenyl)octan-1-one | HCID 18470194 | — |
Reaction Steps
To a stirring suspension of aluminium chloride (33.6 g) in dry dichloromethane (474 ml) was added 8-bromo-n-octanoyl chloride (67.8 g) over 10 min. Chlorobenzene (123 ml) was then added over 10 min and the mixture allowed to stir at 25° C. for 74 h and stood for 64 h. The mixture was poured into ice/water (540 ml) and diethyl ether (1.3 L). The organic layer was removed and was washed with water (540 ml), saturated sodium hydrogen carbonate (540 ml), water (400 ml) and brine (400 ml) and dried over magnesium sulfate. Removal of the organic layer under reduced pressure and chromatography of the residue on silica gel using 5% ethyl acetate in hexane gave 8-bromo-1-(4-chlorophenyl)octan-1-one (35.5 g). 1H-NMR (CDCl3) δ 1.2-1.6 (6H, m), 1.6-1.95 (4H, m), 2.95 (2H, t), 3,42 (2H, t), 7.43 (2H, m) and 7.90 (2H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06417192B1 |
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| Source dataset | uspto-grants-2002_07 |
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| ORD ID | ord-1eacd88017284f9b87750181242571e7 |
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| Source note | uspto-grants-2002_07 |
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