HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491269Generated: October 26, 2026
2-Chlorothiazole → 1-(2-Chlorothiazol-5-yl)ethanone
https://huagongshe.com/reaction/491269
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chlorothiazole | HCID 76429 | — |
| Reactant | N-Methoxy-N-methylacetamide | HCID 537505 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(2-Chlorothiazol-5-yl)ethanone | HCID 51777311 | 73% |
Reaction Steps
A solution of 2-chlorothiazole (2.5 g, 21 mmol) in THF (10 mL) was added dropwise to a chilled (−75° C.) 2.5 M hexanes solution of n-BuLi (9.2 mL, 23 mmol) in THF (70 mL). After the addition was complete the reaction mixture was stirred for 1 hr. Then a solution of N-methoxy-N-methylacetamide (2.4 g, 23 mmol) in THF (5 mL) was added. The reaction was allowed to stir overnight while warming to 25° C. The reaction was diluted with H2O and thrice extracted with ethyl ether. The organic portions were combined, washed with brine and then dried (Na2SO4). Filtration and removal of solvent gave a residue that was purified by flash chromatography on silica eluting with 5 percent Et2O in pentane, affording product as a white solid, 2.5 g, 15.5 mmol, 73 percent yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07531482B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-3e95e4c4c79240cb8344f791c8b89da2 |
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| Source note | uspto-grants-2009_05 |
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