HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1764665Generated: October 31, 2026
1,3-Dibromopropane → HCID 22768839, compound
https://huagongshe.com/reaction/1764665
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,3-Dibromopropane | HCID 8001 | — |
| Reactant | Dibutylamine | HCID 8148 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 22768860 | HCID 22768860 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 22768839 | HCID 22768839 | — |
Reaction Steps
To a solution of 0.85 g. (0.0024 mol.) of 3-(4-hydroxyphenylsulfonyl)-2-phenylbenzofuran in 25 ml. of dry acetone was added 0.96 g. (0.0048 mol.) of 1,3-dibromopropane and 0.66 g. (0.0048 mol.) of potassium carbonate. The mixture was refluxed for ca. 12 hours, then an additional 0.4 g. of 1,3-dibromopropane, 0.3 g. of potassium carbonate and 25 ml. of dry acetone were added and the mixture was refluxed for 5 hours. The reaction mixture was filtered and the solvent was removed in vacuo to give a residue which was dissolved in 2-4 ml. of ethanol to which 22-24 ml. of freshly distilled di-n-butylamine was added. The mixture was heated at 130° for 4 hours, then cooled and diluted with ethanol. The solvent and excess amine were removed by evaporation to give 0.23 g. of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04117128 |
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| Source dataset | uspto-grants-1978_09 |
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| ORD ID | ord-1d2078a83b194665bad2ffd971bf55d7 |
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| Source note | uspto-grants-1978_09 |
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