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Water → 5-(Benzyloxy)-2-tert-butylpyridine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | 5-(Benzyloxy)-2-bromopyridine | HCID 16094696 | — |
| 反応物 | HCID 178418310 | HCID 178418310 | — |
| 反応物 | HCID 178418546 | HCID 178418546 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 5-(Benzyloxy)-2-tert-butylpyridine | HCID 20709505 | — |
反応手順
To a stirred solution of copper (I) cyanide (18.31 g) in dry THF (400 ml) was added, at −78 C., tertbutylmagnesium chloride (1M in THF, 409 ml). The reaction mixture was stirred at this temperature for 15 min before slowly adding a solution of 2-bromo-5-[(phenylmethyl)oxy]pyridine (13.5 g) in THF. This was stirred for 2 h at −78 C. before warming to 25-30 C. and stirring for a further 20 h. The reaction mixture was poured into water and extracted with ethyl acetate. This was concentrated in vacuo and purified through silica, eluting with 0-2% ethyl acetate in hexane. Appropriate fractions were combined and concentrated in vacuo to yield the title compound, 6.3 g
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09447074B2 |
| 出典データセット | uspto-grants-2016_09 |
| ORD ID | ord-cfc9ccb219cb4008b2f12e8507058a75 |
| 出典メモ | uspto-grants-2016_09 |