HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253688Generated: October 26, 2026
1,4-Dibromobutane → 6-(4-Bromobutyloxy)indanone
https://huagongshe.com/reaction/253688
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,4-Dibromobutane | HCID 8056 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 6-Hydroxy-1-indanone | HCID 7020659 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 6-(4-Bromobutyloxy)indanone | HCID 11550940 | 65.4% |
Reaction Steps
A mixture of 6-hydroxyindan-1-one (100 gm, 0.675 mol), potassium carbonate (96 gm, 0.695 mol), 1,4-dibromo butane (365 gm, 1.69 mol) and tetrabutyl ammonium bromide in acetone was introduced in to a three necked round bottomed flask filtered with a water condenser and a mechanical stirrer. The mixture was brought to a temperature 65° C. and maintained at 65° C. for nine hours and then distilled off solvent, diluted with water (400 ml). The aqueous layer was extracted with ethyl acetate, and the extract was washed with water, dried and evaporated in the rotavapour under reduced pressure to get a residue which on crystallization from isopropyl ether gave 125 gm of 6-(4-bromo butoxy)-indan-1-one of the formula 3
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07872132B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-714eff7f063b4ac3ad5ae949c4eac40d |
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| Source note | uspto-grants-2011_01 |
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