HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515457Generated: October 25, 2026
Hexane → 2-(4-Bromophenyl)propane-1,3-diol
https://huagongshe.com/reaction/515457
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Potassium sodium tartarate | HCID 9855836 | — |
| Reactant | Diethyl 4-bromophenylmalonate | HCID 10519382 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-(4-Bromophenyl)propane-1,3-diol | HCID 21866701 | 37.4% |
Reaction Steps
To a solution of diethyl 2-(4-bromophenyl)malonate (18.1 g, 57.5 mmol) in ether (285 ml) was added 0.98M-diisobutylaluminium hydride in hexane (259 ml, 254 mmol) at 0° C. under nitrogen atmosphere. The resulting mixture was stirred at 0° C. for 4 hours. Aqueous potassium sodium tartrate (0.57M, 500 ml) was added to the reaction mixture for quenching the aluminum reagent and the mixture was stirred for 14 hours. The organic layer was extracted with ethyl acetate and dried over sodium sulfate. After concentration, the residue was purified by silica gel column chromatography (eluant: hexane/ethyl acetate=40/60 to ethyl acetate only) to afford 2-(4-bromophenyl)propane-1,3-diol as white solid (4.97 g, 37%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09108957B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-073ca934b9104bed9e97062c70542276 |
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| Source note | uspto-grants-2015_08 |
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