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Phosphine, triphenyl-, hydrobromide → (2,4-Dimethyl-5-methoxy-3-thenyl)triphenylphosphonium bromide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Phosphine, triphenyl-, hydrobromide | HCID 517696 | — |
| 反応物 | 2,4-Dimethyl-3-hydroxymethyl-5-methoxythiophene | HCID 12875268 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | (2,4-Dimethyl-5-methoxy-3-thenyl)triphenylphosphonium bromide | HCID 86735242 | — |
反応手順
6.1 G. (35.5 mmol) of 2,4-dimethyl-3-hydroxymethyl-5-methoxythiophene were added at 35° C. with vigorous stirring to a suspension of 13.4 g. (39.0 mmol) of triphenylphosphonium bromide in 250 ml. of acetonitrile. The deep purple color which was formed immediately, disappeared after some minutes. The reaction mixture was stirred for 3 hrs. The solvent was evaporated to a volume of about 25 ml. and an excess of cold ether was added. The solvent then was decanted from the resulting oily precipitate which was dissolved in warm acetone and again precipitated by adding cold ether. The solvent was decanted and the resulting oily residue was dried in high vacuum to yield (2,4-dimethyl-5-methoxy-3-thenyl)triphenylphosphonium bromide.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04256878 |
| 出典データセット | uspto-grants-1981_03 |
| ORD ID | ord-7a9da052dcdf45dbb864d6811b5e88e1 |
| 出典メモ | uspto-grants-1981_03 |