Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylthiazole | HCID 12748 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-(benzo[d][1,3]dioxol-5-yl)-N-methoxy-N-methylacetamide | HCID 14918161 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 23154591 | HCID 23154591 | 91.5% |
Reaction Steps
A 2.6M solution of n-butylithium in hexane (34 ml) was dropped into a solution of 4-methylthiazole (8.0 g) of tetrahydrofuran (150 ml) at −70° C. and the mixture was stirred for 30 minutes. Further, a solution of 2-benzo(1,3)dioxol-5-yl-N-methoxy-N-methylacetamide (20.0 g) in tetrahydrofuran (20 ml) was dropped therein and the mixture was stirred for 1 hour. This solution, to which a saturated aqueous solution of ammonium chloride was added, was extracted with ethyl acetate, and after the organic layer was dried over anhydrous magnesium sulfate, the solvent was evaporated. The resultant residue was purified by silica gel flash column chromatography using a mixed solvent of ethyl acetate and hexane to yield 2-benzo(1,3)dioxol-5-yl-1-(4-methylthiazol-2-yl)ethanone (19.3 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07678810B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-a4af4b97172f4577bbe41f5b7c45df80 |
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| Source note | uspto-grants-2010_03 |
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