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Methyl chloroformate → Carbamic acid, [(2-chlorophenyl)sulfonyl]-, methyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Methyl chloroformate | HCID 6586 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 2-Chlorobenzenesulfonamide | HCID 81410 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | Carbamic acid, [(2-chlorophenyl)sulfonyl]-, methyl ester | HCID 4389137 | — |
反応手順
To 25.0 g 2-chloro-benzenesulfonamide was added 75 mL acetonitrile and 45.2 mL (2.5 eq) triethylamine. The mixture was cooled with an ice bath and 15.1 mL methyl chloroformate was slowly added dropwise. The mixture was stirred overnight at room temperature and concentrated in vacuo. Water was added and de aqueous layer was washed two times with ether. Acidification of the aqueous layer with 2 M HCl led to formation of a white precipitate. The suspension was filtered, the residue was washed with H2O and dried in vacuo to yield 19.1 g of a white solid. 1H NMR (400 MHz, DMSO-d6) δ 3.58 (s, 3H), 7.52-7.61 (m, 1H), 7.62-7.72 (m, 2H), 8.10 (dd, J=8 and 1.5 Hz, 1H), 12.42 (br s, 1H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08722887B2 |
| 出典データセット | uspto-grants-2014_05 |
| ORD ID | ord-71f068dc5a4c419ba1ea5b2310a5943a |
| 出典メモ | uspto-grants-2014_05 |