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N-Butylchlorodimethylsilane → (4-Bromophenylethynyl)-n-butyldimethylsilane
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | N-Butylchlorodimethylsilane | HCID 66079 | — |
| 反応物 | Benzene, 1-bromo-4-ethynyl- | HCID 136603 | — |
| 反応物 | HCID 178418365 | HCID 178418365 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | (4-Bromophenylethynyl)-n-butyldimethylsilane | HCID 66905447 | 90% |
反応手順
i-propylmagnesiumbromide (0.67 M/THF solution, 3.10 mL, 2.1 mmol) was added dropwise to THF solution (15 mL) of 1-bromo-4-ethynylbenzene (382 mg, 2.0 mmol) at 0° C. After the mixture was stirred for 20 minutes, an ice water bath was removed. After stirring at room temperature for 10 minutes, n-butyldimethylsilyl chloride (0.69 mL, 4.0 mmol) was added to the mixture. After stirring for 2 hours, the reaction was terminated by the addition of saturated ammonium chloride solution (5 mL). The reaction mixture was extracted with ethyl acetate, and it was concentrated and thereafter purified by means of flash column chromatography to obtain (4-bromophenylethynyl)-n-butyldimethylsilane (530 mg, isolated yield: 90%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08153835B2 |
| 出典データセット | uspto-grants-2012_04 |
| ORD ID | ord-1873323f6ad14c0abe110cf23c88ae64 |
| 出典メモ | uspto-grants-2012_04 |