Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Triphenylphosphine → 3'-(Bromomethyl)-5'-(trifluoromethyl)biphenyl-4-carbonitrile
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Triphenylphosphine | HCID 11776 | — |
| 반응물 | N-bromobutanimide | HCID 67184 | — |
| 반응물 | 3'-(Hydroxymethyl)-5'-(trifluoromethyl)biphenyl-4-carbonitrile | HCID 58993672 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 3'-(Bromomethyl)-5'-(trifluoromethyl)biphenyl-4-carbonitrile | HCID 58993490 | 64% |
반응 단계
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).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08383821B2 |
| 출처 데이터셋 | uspto-grants-2013_02 |
| ORD ID | ord-1b24b27c1ecc4ddebe9a66406204f0cb |
| 출처 메모 | uspto-grants-2013_02 |