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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2177345Generated: October 30, 2026

Diethyl Ether → (3-(4-Ethylphenyl)-5-methylthiophen-2-yl)methanol

https://huagongshe.com/reaction/2177345

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantMethyl 3-(4-ethylphenyl)-5-methylthiophene-2-carboxylateHCID 90418379—
SolventTetrahydrofuranHCID 8028—
Product(3-(4-Ethylphenyl)-5-methylthiophen-2-yl)methanolHCID 90418314—

Reaction Conditions

Temperature0 °C

Reaction Steps

Into a 100-mL 3-necked round-bottom flask (1 atm) purged and maintained with an inert atmosphere of nitrogen, was placed methyl 3-(4-ethylphenyl)-5-methylthiophene-2-carboxylate (1.5 g, 5.76 mmol), anhydrous ether (50 mL). This was followed by the addition of a solution of LiAlH4 (1 M in THF, 7.9 mL, 7.86 mmol) in tetrahydrofuran dropwise with stirring at 0° C. The resulting solution was stirred for 2.0 h at 25° C. The reaction progress was monitored by LCMS/TLC (ethyl acetate/petroleum ether=1:6). The reaction was then quenched by the addition of 10 mL of water and 5 mL of 2N HCl. The resulting solution was extracted with 3×20 mL of ethyl acetate and the organic layers combined and dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1:4). This resulted in 1.26 g (94%) of (3-(4-ethylphenyl)-5-methylthiophen-2-yl)methanol as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067898B1
Source datasetuspto-grants-2015_06
ORD IDord-e88ceafe566a43b8849957e36b132779
Source noteuspto-grants-2015_06