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Lawesson's reagent → 4-bromo-3-chloro-N-trimethylsilanylmethylthiobenzamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Lawesson's reagent | HCID 87949 | — |
| 反応物 | 4-bromo-3-chloro-N-trimethylsilanylmethyl-benzamide | HCID 66836699 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 4-bromo-3-chloro-N-trimethylsilanylmethylthiobenzamide | HCID 86685705 | 96.1% |
反応手順
To a solution of 4-bromo-3-chloro-N-trimethylsilanylmethyl-benzamide (Example I12) (4.6 g) in toluene (150 ml) was added 2,4-bis(4-methoxyphenyl)-1,3,2,4-dithiadiphosphetane 2,4-disulfide (Lawesson reagent) (5.8 g). The reaction mixture was stirred at ambient temperature for 30 minutes and then at 110° C. for 1.5 hours. The reaction mixture was concentrated and the residue purified by chromatography on silica gel (eluent: ethyl acetate/heptanes 1:5) to give 4-bromo-3-chloro-N-trimethylsilanylmethylthiobenzamide (4.64 g). 1H-NMR (400 MHz, CDCl3): 1H-NMR (400 MHz, CDCl3): 7.60 (d, 1H), 7.45 (s, 1H), 7.30 (s, 1H), 7.25 (d, 1H), 3.33 (d, 2H), 0.00 (s, 9H) ppm.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08946447B2 |
| 出典データセット | uspto-grants-2015_02 |
| ORD ID | ord-e6ed26e2d401498fb0ef9332e4a00962 |
| 出典メモ | uspto-grants-2015_02 |