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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1759202Generated: October 31, 2026

Water → [3-(1H-Pyrrol-1-yl)phenyl]methanol

https://huagongshe.com/reaction/1759202

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-(3-Ethoxycarbonylphenyl)pyrroleHCID 4763724—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantOxolane--water (1/1)HCID 21881883—
SolventDiethyl EtherHCID 3283—
Product[3-(1H-Pyrrol-1-yl)phenyl]methanolHCID 2776531111.7%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04339457
Source datasetuspto-grants-1982_07
ORD IDord-70b7a0ef381e4083b833887a9f009ef8
Source noteuspto-grants-1982_07