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Methanesulfonyl chloride → N-(3-bromopropyl)methanesulfonamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Methanesulfonyl chloride | HCID 31297 | — |
| 反応物 | 2-Bromopropan-1-amine hydrobromide | HCID 12570703 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | N-(3-bromopropyl)methanesulfonamide | HCID 11218181 | — |
反応手順
To a cooled solution of 2-bromopropylamine hydrobromide (43.8 g., 0.20 mole) in pyridine (100 ml.) was added over a period of 40 minutes methanesulfonyl chloride (15.2 ml., 0.20 mole). The reaction mixture was stirred for 15 minutes and then diluted with ether. The remaining solid was filtered off, washed with about 200 ml. of acetone. The filtrate and washes were concentrated in vacuo. The residue was extracted with three 100 ml. portions of acetone. Upon evaporation of the acetone, 30.4 g. of a thick oil representing the title compound. The product was confirmed by infrared analysis and nuclear magnetic resonance.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04071349 |
| 出典データセット | uspto-grants-1978_01 |
| ORD ID | ord-9b9097d578f943189e34367f77723d0e |
| 出典メモ | uspto-grants-1978_01 |