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HRID 2262864생성일: 2026년 10월 26일

Nitric Acid → 4,5-Dimethoxy-2-nitrophenol

https://huagongshe.com/reaction/2262864

반응식

참여 물질

역할이름HCID투입량
반응물Nitric AcidHCID 944—
반응물3,4-DimethoxyphenolHCID 16251—
용매Acetic AcidHCID 176—
생성물4,5-Dimethoxy-2-nitrophenolHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07851501B2
출처 데이터셋uspto-grants-2010_12
ORD IDord-470721f2c58e44d09b9fdde48812aa67
출처 메모uspto-grants-2010_12