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2,3-Dibromopropene → 7-[(2-bromoallyl)oxy]-4-methyl-2H-chromen-2-one
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2,3-Dibromopropene | HCID 10552 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 4-Methylumbelliferone | HCID 5280567 | — |
| 溶媒 | Acetone | HCID 180 | — |
| 生成物 | 7-[(2-bromoallyl)oxy]-4-methyl-2H-chromen-2-one | HCID 342449 | 89% |
反応手順
4-Methyl-7-hydroxycoumarin (2.00 g., 11.4 m mole) was refluxed with freshly-distilled 2,3-dibromopropene (2.72 g., 13.6 m mole), anhydrous potassium carbonate (3.15 g., 22.8 m mole), and acetone (80 ml.) for four hours. The reaction mixture was treated as described for the preparation of Example I, Part 1-A to obtain 4-methyl-7-(2'-bromoallyloxy) coumarin as an off-white solid (3.70 g.) that contained some excess 2,3-dibromopropene. Recrystallization of a portion (500 mg.) from ligroin (b.p. 100°-120° C.) gave needles (394 mg., 89% yield) of m.p. 109.5°-110.5° C. An analytical sample of m.p. 110°-111° C. was obtained by recrystallization from methanol.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04235781 |
| 出典データセット | uspto-grants-1980_11 |
| ORD ID | ord-119bd61beb0d4d279285b1bd4e15074f |
| 出典メモ | uspto-grants-1980_11 |