HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 653745Generated: October 31, 2026
Oxalyl chloride → 5-Bromo-1,2,3,4-tetrahydronaphthalen-1-one
https://huagongshe.com/reaction/653745
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 4-(2-Bromophenyl)butanoic acid | HCID 13330230 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 5-Bromo-1,2,3,4-tetrahydronaphthalen-1-one | HCID 10889572 | 92% |
Reaction Steps
To a benzene solution (60 ml) of 4-(o-bromophenyl) butyric acid (5 g) was added oxalyl chloride (3.6 ml) and the reaction refluxed for 11/2 hrs. The solution was evaporated to dryness, the residue was dissolved in CH2Cl2 (50 ml) then cooled to 0° C., followed by the addition of AlCl3 (3.1 g). The mixture was stirred at 0° C. warming to room temperature overnight. The reaction was poured onto ice, then extracted with CH2Cl2. The organic layer was separated, washed with 1N NaOH, then brine, separated, dried (MgSO4), filtered and evaporated affording the desired product (4.26 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05128362 |
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| Source dataset | uspto-grants-1992_07 |
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| ORD ID | ord-a533272a5fe5427ebb632e7b35cfc897 |
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| Source note | uspto-grants-1992_07 |
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