HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 974044Generated: October 29, 2026
Hydrochloric Acid → 1-(2-Fluoro-4-biphenylyl)ethyl-2-dimethylaminothiazole
https://huagongshe.com/reaction/974044
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Tetrabutylammonium | HCID 16028 | — |
| Reactant | 4-(1-(2-Fluoro-4-biphenyl)ethyl)-2-methylaminothiazole | HCID 124238 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(2-Fluoro-4-biphenylyl)ethyl-2-dimethylaminothiazole | HCID 15676021 | 85% |
Reaction Steps
To 4-(1-(2-fluoro-4-biphenylyl)ethyl)-2-methylaminothiazole(415 mg, 1.33 mmol) in benzene (6 ml) was added methyl iodide (370 mg, 2.61 mmol), tetra-n-butyl ammonium hydrogene sulfate (435 mg, 1.33 mmol) and 50% NaOH aq. (3 ml), then the mixture was stirred at room temperature overnight. The reaction mixture was diluted with water, then acidified with 2N-HCl to pH 6 and the aqueous solution was extracted with benzene. The extracts were washed with water, dried and then evaporated under reduced pressure to a residue, which chromatographed to afford 4-(1-(2-fluoro-4-biphenylyl)ethyl)-2-dimethylaminothiazole (369 mg, 85% yield): NMR(CDCl3)δ 1.62(d, 3H), 3.06(s, 6H), 4.09(q, 1H), 6.06(s, 1H), 7.02-7.63(m, 8H) ppm; IR(neat) 2950, 1620, 1550, 1420, 1340 cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05066666 |
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| Source dataset | uspto-grants-1991_11 |
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| ORD ID | ord-e391e34c56674ed4a8cb783ceb4b593c |
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| Source note | uspto-grants-1991_11 |
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