HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 728074Generated: October 29, 2026
Ethylene → 8-Bromo-1,2,3,4-tetrahydronaphthalen-2-one
https://huagongshe.com/reaction/728074
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethylene | HCID 6325 | — |
| Reactant | 2-Bromophenylacetyl chloride | HCID 4138386 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 8-Bromo-1,2,3,4-tetrahydronaphthalen-2-one | HCID 4136187 | — |
Reaction Steps
83.5 g of aluminum chloride (0.63 mmol) were introduced into 1.8 liters of methylene chloride at 0°-+5° C. 105 g (0.49 mole) of 2-bromophenyl-acetyl chloride (dissolved in 200 ml of methylene chloride) were added dropwise at 0°-+5° C. over 30 minutes. After stirring for 30 minutes at 0°-+5° C., 50 g of ethylene were passed in at such a rate that the reaction temperature did not exceed +10° C. The mixture was stirred for a further 2 hours at 20°-+25° C. The aluminum complex was decomposed by careful addition of 500 ml of ice water, the phases were separated, and the aqueous phase was extracted with 250 ml of methylene chloride. The title compound was obtained from the dried methylene chloride phase in a yield of 109 g as a yellow oil (content according to GC 97%) and employed without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05047422 |
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| Source dataset | uspto-grants-1991_09 |
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| ORD ID | ord-466ce25420ef495b813c28d665abd854 |
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| Source note | uspto-grants-1991_09 |
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