Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Nitric Acid → 4,5-Dimethoxy-2-nitrophenol
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Nitric Acid | HCID 944 | — |
| 반응물 | 3,4-Dimethoxyphenol | HCID 16251 | — |
| 용매 | Acetic Acid | HCID 176 | — |
| 생성물 | 4,5-Dimethoxy-2-nitrophenol | HCID 297121 | — |
반응 단계
In SCHEME 9 3,4-dimethoxyphenol (36) is selectively nitrated with 70% HNO3 in AcOH to give 4,5-dimethoxy-2-nitrophenol (37) which is further converted to the corresponding triflate (38) with trifluoromethylsulfonic anhydride (Tf2O) and pyridine in dichloromethane. Triflate (38) is reacted under inert conditions with a boronic acid of general type (31) under Suzuki-type basic conditions (Pd(PPh3)4 and aqueous potassium phosphate in toluene) to a biaryl of type (39). Biaryl (39) is further hydrolized with aqueous lithium hydroxide in THF and MeOH or MeCN to give the corresponding carboxylic acid (40) which is converted to a building block of type (41) by reaction with oxalyl chloride in anhydrous dichloromethane.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07851501B2 |
| 출처 데이터셋 | uspto-grants-2010_12 |
| ORD ID | ord-470721f2c58e44d09b9fdde48812aa67 |
| 출처 메모 | uspto-grants-2010_12 |