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Acetonitrile → 11-Carbethoxyundecyltriphenylphosphonium bromide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acetonitrile | HCID 6342 | — |
| 反応物 | Triphenylphosphine | HCID 11776 | — |
| 反応物 | Ethyl 11-bromoundecanoate | HCID 235144 | — |
| 生成物 | Phosphonium | HCID 5460504 | — |
| 生成物 | 11-Carbethoxyundecyltriphenylphosphonium bromide | HCID 19063384 | 83% |
反応手順
Ethyl-11-bromoundecanoate (36.0 g, 123 mmol) and acetonitrile (200 ml) were placed in a flame-dried three-neck 500 ml round-bottomed flask equipped with a reflux condenser. Triphenyl phosphine (35.5 g, 135 mmol) was added to the solution and the reaction mixture was refluxed for 36 hours under anhydrous conditions. After the reaction mixture had cooled to room temperature, the acetonitrile was removed under reduced pressure. The crude product was triturated with ether. The solid was filtered and washed with ether to yield a pure compound 3, 11-carbethoxyundecyltriphenylphosphonium bromide (56.69 g, 83% yield).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05795561 |
| 出典データセット | uspto-grants-1998_08 |
| ORD ID | ord-b5936d24b55a4664b96b202ddd194937 |
| 出典メモ | uspto-grants-1998_08 |