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Triethylamine → 2-[(Methylsulfonyl)oxy]-5-hexynenitrile
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Methanesulfonyl chloride | HCID 31297 | — |
| 反応物 | 2-Hydroxy-5-hexynenitrile | HCID 13044948 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 2-[(Methylsulfonyl)oxy]-5-hexynenitrile | HCID 13044949 | 87.4% |
反応手順
A mixture of 2-hydroxy-5-hexynenitrile (8.0 g, 73.3 mmol) and dry triethylamine (10.1 g, 0.1 mol) in 50 ml of dry CH2Cl2 was treated with a solution of methanesulfonyl chloride (10.3 g, 90 mmol) in 50 ml of CH2Cl2, at 0° C. for 11/2 h. The reaction mixture was diluted with CH2Cl2, washed twice with cold 1.0N H2SO4, twice with water, and dried over MgSO4. The filtered CH2Cl2 solution was concentrated at 40° C./30 mm to give 12 g of pale yellow liquid. Purification of this material on 220 g of silica gel and eluted with ether-petroleum ether (1:1 parts by volume) gave 8.7 g (56% by weight yield from pentynal) of 2-[(methylsulfonyl)]-5-hexynenitrile as a colorless liquid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04500462 |
| 出典データセット | uspto-grants-1985_02 |
| ORD ID | ord-bc5064ebef77485db2f8886dbf5b8c68 |
| 出典メモ | uspto-grants-1985_02 |