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Dimethylformamide → 3-(3-Cyclopentyloxy methoxyphenyl)-3-ethynylcyclohexan-1-one
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | Potassium Fluoride | HCID 522689 | — |
| 反応物 | 3-(3-Cyclopentyloxy-4-methoxyphenyl)-3-trimethylsilylethynylcyclohexan-1-one | HCID 53983747 | — |
| 生成物 | 3-(3-Cyclopentyloxy methoxyphenyl)-3-ethynylcyclohexan-1-one | HCID 53769136 | — |
反応手順
A mixture of potassium fluoride (900 mg, 15.6 mmol) and 3-(3-cyclopentyloxy-4-methoxyphenyl)3-trimethylsilylethynyl cyclohexan-1-one (0.3 g, 0.78 mmol) was stirred in dry N,N-dimethylformamide (3 mL) under an argon atmosphere. After 18 h, the solvent was removed in vacuo, the residue was partitioned between water and ethyl acetate, the aqueous layer was extracted twice with ethyl acetate, the combined extract was dried (magnesium sulfate) and was evaporated. Purification by flash chromatography, eluting with 4:1 hexanes/ethyl acetate provided a clear colorless oil . Anal. (C20H24O3 ·1/10H2O) calcd: C 76.45,H 7.76; found: C 76.32,H 7.60.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05892098 |
| 出典データセット | uspto-grants-1999_04 |
| ORD ID | ord-2a9161eed8084afc9d4b632dfb550c5f |
| 出典メモ | uspto-grants-1999_04 |