Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1-(3-Ethoxycarbonylphenyl)pyrrole | HCID 4763724 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | Oxolane--water (1/1) | HCID 21881883 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | [3-(1H-Pyrrol-1-yl)phenyl]methanol | HCID 2776531 | 111.7% |
Reaction Steps
To a stirred mixture of 4.8 grams of lithium aluminum hydride in 150 ml of dry diethyl ether was added dropwise 23.2 grams (0.108 mole) of ethyl 3-(pyrrol-1-yl)benzoate in 160 ml of dry diethyl ether. The complete addition required 45 minutes. After this time the reaction mixture was heated under reflux for 45 minutes then allowed to cool to ambient temperature where it stood for 16 hours. The excess lithium aluminum hydride was decomposed by the careful addition of 20 ml of 50% (v/v) water-tetrahydrofuran. The addition required 20 minutes as the reaction mixture temperature was kept below 25° C. The reaction mixture was poured into 300 ml of water and the diethyl ether layer separated. The aqueous layer was extracted with three portions of 200 ml each of diethyl ether. The combined ether layers were washed with water and dried with magnesium sulfate. The mixture was filtered and the filtrate concentrated under reduced pressure to give 20.9 grams of 3-(pyrrol- 1-yl)phenylmethanol; mp 64°-67° C. The ir spectrum was consistent with the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04339457 |
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| Source dataset | uspto-grants-1982_07 |
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| ORD ID | ord-70b7a0ef381e4083b833887a9f009ef8 |
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| Source note | uspto-grants-1982_07 |
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