돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 494853생성일: 2026년 10월 25일

Sodium Carbonate → 4'-Hydroxy-5'-iodo-3'-methyl-1,1'-biphenyl-4-carbonitrile

https://huagongshe.com/reaction/494853

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물Sodium SulfiteHCID 24437—
반응물1,1,3,3-TetramethylguanidineHCID 66460—
반응물N-IodosuccinimideHCID 120273—
반응물Monobasic potassium phosphateHCID 516951—
반응물4'-Hydroxy-3'-methyl-[1,1'-biphenyl]-4-carbonitrileHCID 22274497—
용매Diethyl EtherHCID 3283—
용매DimethylformamideHCID 6228—
생성물4'-Hydroxy-5'-iodo-3'-methyl-1,1'-biphenyl-4-carbonitrileHCID 2227458317%

반응 단계

4′-hydroxy-3′-methyl-1,1′-biphenyl-4-carbonitrile (875 mg, 4.18 mmol) was dissolved into DMF (20 mL) and treated with N-iodosuccinimide (1.012 g, 4.5 mmol). The solution was stirred at room temperature for four days. Then the mixture was stirred with tetramethylguanidine (1 mL) for ten minutes, poured into an aqueous mixture of Na2SO3 and Na2CO3, adjusted to pH 9 with aqueous potassium dihydrogen phosphate, and diluted with ether. The gum which separated from the biphasic mixture was dissolved into EtOAc and added to a rapidly stirred mixture of the aqueous phase and ether. The organic phase was separated, filtered, combined with the original ethereal phase, concentrated, and chromatographed through silica with a 50% to 100% gradient of CH2Cl2/hexanes to provide the title compound as an off-white powder (17% yield). MS (ESI APCI negative ion detection) m/z 334 (M−H)−; 1HNMR (300 MHz, CDCl3) δ 2.38 (s, 3H), 7.26 (s, 1H), 7.33 (d, 1H), 7.60 (d, 2H), 7.66-7.74 (m, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07538138B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-1cbe502cab4a40aaa92da89356bd699c
출처 메모uspto-grants-2009_05