Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Trimethyl borate → 4-(1,3-Dioxolan-2-yl)-3-(trifluoromethyl)phenylboronic acid
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Trimethyl borate | HCID 8470 | — |
| 반응물 | 2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane | HCID 5017741 | — |
| 반응물 | 2-[4-Iodo-2-(trifluoromethyl)phenyl]-1,3-dioxolane | HCID 58276681 | — |
| 반응물 | HCID 178418918 | HCID 178418918 | — |
| 생성물 | 4-(1,3-Dioxolan-2-yl)-3-(trifluoromethyl)phenylboronic acid | HCID 58276450 | — |
반응 단계
The title compound was prepared from 2-[4-iodo-2-(trifluoromethyl)phenyl]-1,3-dioxolane (Example I-IX-7) according to the procedure described for Example V-18, with the following exceptions: the aryl iodide and i-PrMgCl were aged 45 min before introduction of the electrophile (instead of 30 min); trimethyl borate was used as the electrophile (instead of 2-isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane); the dried organic extracts were concentrated to dryness and triturated with Et2O/hexanes (instead of flash chromatography). White solid. LC/MS (method A) 2.22 min, m/z 417 ({2[M-gylcol]-H2O}—H, 23%), 217 ([M-glycol]-H, 57%), 189 (100%, −ve ion).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08822518B2 |
| 출처 데이터셋 | uspto-grants-2014_09 |
| ORD ID | ord-d0034df33c7d499db45ff337c85d8550 |
| 출처 메모 | uspto-grants-2014_09 |