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4-Acetylmorpholine → trifluoro-methanesulfonic acid 2-morpholin-4-yl-4-oxo-4H-chromen-8-yl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-Acetylmorpholine | HCID 15543 | — |
| 反応物 | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| 反応物 | Methyl 2-hydroxy-3-(trifluoromethylsulfonyloxy)benzoate | HCID 11616395 | — |
| 生成物 | trifluoro-methanesulfonic acid 2-morpholin-4-yl-4-oxo-4H-chromen-8-yl ester | HCID 11603298 | — |
反応手順
Condensation of the lithium enolate of N-acetyl morpholine (2.2 ml) with methyl 2-hydroxy-3-trifluoromethanesulfonyloxy-benzoate (3.56 g, 11.9 mmol) yielded the salicylacatamide (3.6 g). Cyclodehydration of the product with trifluormethanesulfonic anhydride (5.5 ml) as described above yielded the product as a colourless solid (1.21 g).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06977255B2 |
| 出典データセット | uspto-grants-2005_12 |
| ORD ID | ord-555a1e808deb49deb54b2b484d0caabb |
| 出典メモ | uspto-grants-2005_12 |