HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2295852Generated: October 30, 2026
Water → [2-Methyl-3-(thiophen-2-yl)phenyl]methanol
https://huagongshe.com/reaction/2295852
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | 2-Methyl-3-(thiophen-2-yl)benzoic acid | HCID 13243417 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [2-Methyl-3-(thiophen-2-yl)phenyl]methanol | HCID 13243418 | 99.8% |
Reaction Steps
Under an argon atmosphere, a stirred solution of 5.7 g (0.026 mol) of 2-methyl-3-(2-thienyl)benzoic acid in 50 mL of tetrahydrofuran was cooled to 0° C.±2° C. To this solution was added dropwise 4.4 g (0.051 mol, 51.3 mL of a 1.0 M solution) of borane tetrahydrofuran complex. The addition was made over 35 minutes. The reaction mixture was stirred for 0.5 hour at ambient temperature, then for two hours at reflux temperature. The reaction mixture was cooled, and 100 mL of diethyl ether saturated with water, then 20 mL of water, were cautiously added. The mixture was transferred to a separatory funnel containing 50 mL of ice, and was saturated with solid sodium chloride, and extracted with three portions of 200 mL each of diethyl ether. The combined extracts were dried with magnesium sulfate, filtered, and the filtrate concentrated under reduced pressure to give 5.3 g of 2-methyl-3-(2-thienyl)phenylmethanol as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04426524 |
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| Source dataset | uspto-grants-1984_01 |
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| ORD ID | ord-2de8797c9f22414bbbeedc2d225c56dc |
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| Source note | uspto-grants-1984_01 |
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