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Triphenylphosphine → 3'-(Bromomethyl)-5'-(trifluoromethyl)biphenyl-4-carbonitrile
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triphenylphosphine | HCID 11776 | — |
| 反応物 | N-bromobutanimide | HCID 67184 | — |
| 反応物 | 3'-(Hydroxymethyl)-5'-(trifluoromethyl)biphenyl-4-carbonitrile | HCID 58993672 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 3'-(Bromomethyl)-5'-(trifluoromethyl)biphenyl-4-carbonitrile | HCID 58993490 | 64% |
反応手順
N-bromosuccinimide (2.24 g, 12.6 mmol) was added to a 0° C. solution of 3′-(hydroxymethyl)-5′-(trifluoromethyl)biphenyl-4-carbonitrile (1.66 g, 6.0 mmol) and triphenylphosphine (3.14 g, 12.0 mmol) in THF (100 mL). The reaction was warmed to ambient temperature and stirred for 18 hours. The solvent was evaporated and the residue was purified by chromatography on SiO2 with a gradient of ethyl acetate/hexanes of 5% to 40%. The product 3′-(bromomethyl)-5′-(trifluoromethyl)biphenyl-4-carbonitrile (1.30 g, 64%) was obtained as a white solid. 1H-NMR (CDCl3, 400 MHz) δ 7.65-7.80 (m, 7H), 4.56 (s, 2H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08383821B2 |
| 出典データセット | uspto-grants-2013_02 |
| ORD ID | ord-1b24b27c1ecc4ddebe9a66406204f0cb |
| 出典メモ | uspto-grants-2013_02 |