HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1625767Generated: November 2, 2026
1,3-Dibromobenzene → 3-Bromophenyl-5-ethyl-2-thienylmethanol
https://huagongshe.com/reaction/1625767
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,3-Dibromobenzene | HCID 7927 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 5-Ethyl-2-thiophenecarboxaldehyde | HCID 169830 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Bromophenyl-5-ethyl-2-thienylmethanol | HCID 61100862 | 70.1% |
Reaction Steps
A solution of 1,3-dibromobenzene (3.7 g) in tetrahydrofuran (25 ml) was cooled to −78° C. under argon atmosphere, and thereto was added dropwise n-butyl lithium (2.44 M hexane solution, 5.55 ml). The reaction mixture was stirred at the same temperature for 10 minutes, and thereto was added dropwise a solution of 5-ethyl-2-thiophenecarboxaldehyde (2.0 g) in tetrahydrofuran (10 ml). The mixture was stirred at the same temperature for 30 minutes, and thereto was added a saturated ammonium chloride solution, and the reaction mixture was warmed to room temperature. The mixture was extracted with ethyl acetate, and the extract was dried over magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=97:3-85:15) to give 3-bromophenyl-5-ethyl-2-thienylmethanol (2.97 g) as a pale yellow syrup. APCI-Mass m/Z 279/281 (M+H−H2O).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08785403B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-1edaaae7da114f578cfb77a5432c825f |
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| Source note | uspto-grants-2014_07 |
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