HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2231278Generated: November 1, 2026
Hydrochloric Acid → 3-Methyl-2-phenylthiophene
https://huagongshe.com/reaction/2231278
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2-Bromo-3-methylthiophene | HCID 84314 | — |
| Reactant | HCID 178418255 | HCID 178418255 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 3-Methyl-2-phenylthiophene | HCID 10419681 | — |
Reaction Steps
A stirred mixture of 2-bromo-3-methylthiophene (15.0 g, 0.085 mole) and bis(1,3-diphenylphosphino)propane nickel(II) chloride (0.5 g, 0.009 mole) in diethyl ether (75 mL) was cooled to 0° C. Phenyl magnesium bromide (29.6 mL of a 3M solution in diethyl ether) was added slowly, causing the reaction mixture to reflux. After complete addition, reflux was continued for 15 minutes. The mixture was cooled, and approximately 100 mL of an aqueous 10% hydrochloric acid solution was added. The resultant mixture was extracted with diethyl ether, and the extract was washed with an aqueous saturated sodium bicarbonate solution. The washed extract was dried over anhydrous magnesium sulfate and filtered. The filtrate was evaporated under reduced pressure yielding 17.3 g of 3-methyl-2-phenylthiophene as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04782079 |
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| Source dataset | uspto-grants-1988_11 |
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| ORD ID | ord-54dab1588fa4438292276f99f4aeec1a |
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| Source note | uspto-grants-1988_11 |
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