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Pyridine → 3-Triphenylmethoxy-1-octyne
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Pyridine | HCID 1049 | — |
| 反応物 | Bromotriphenylmethane | HCID 11692 | — |
| 反応物 | 1-Octyn-3-ol | HCID 13166 | — |
| 反応物 | Potassium Bromide | HCID 253877 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 3-Triphenylmethoxy-1-octyne | HCID 12675347 | — |
反応手順
A mixture of 1.26 g. (10.0 mmoles) of 1-octyn-3-ol, 4.85 g. (15.0 mmoles) of triphenylmethyl bromide, and 50 ml. of dry pyridine is heated at 95° C. for 60 minutes with occasional swirling. The solution is cooled, treated with water, and extracted with ether. The extract is washed successively with water and saturated sodium chloride, dried over magnesium sulfate, and concentrated. The crude product is purified by chromatography on Florisil and recrystallization from petroleum ether to give white crystals, m.p. 65°-66° C. λ max. (KBr) 3280 (acetylenic hydrogen), 1605, 1030, and 702 cm-1 (triphenylmethoxy group) .
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04236027 |
| 出典データセット | uspto-grants-1980_11 |
| ORD ID | ord-a0d9e404f94e42e6a0d8bd08988eb914 |
| 出典メモ | uspto-grants-1980_11 |