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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 41333생성일: 2026년 10월 24일

Formaldehyde → 2-Formyl-6-phenylphenol

https://huagongshe.com/ko/reaction/41333

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물(1,1'-Biphenyl)-2-olHCID 7017—
반응물TriethylamineHCID 8471—
반응물Magnesium ChlorideHCID 5360315—
용매Hydrochloric AcidHCID 313—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물2-Formyl-6-phenylphenolHCID 10703100—

반응 조건

온도31.5 °C

반응 단계

Triethylamine (20.2 g, 27.8 mL, 0.20 mol, 2.0 equiv) was added to a solution of 2-phenylphenol (13) (17.0 g, 0.10 mol, 1.0 equiv) in THF (200 mL) followed by solid magnesium chloride (14.3 g, 0.15 mol, 1.5 equiv). The reaction temperature increased from 23 to 40° C. over ˜10 min. The reaction mixture was stirred an additional 10 min during which time a light tan suspension formed. Paraformaldehyde (15.0 g, 0.5 mol, 5.0 equiv) was added and the mixture heated to reflux with formation of a yellow suspension. The mixture was refluxed for 2.5 hr, allowed to slowly cool to room temperature and stirred overnight. The mixture was diluted with EtOAc and 1N HCl (300 mL) with mild cooling to keep the reaction temperature at <25° C. The mixture was transferred to a separatory funnel and shaken with an additional 1N HCl (200 mL). The organic phase was washed with brine (300 mL), dried over Na2SO4, filtered and the solution concentrated under reduced pressure giving a yellow oil that partially crystallized. The oily crystalline material was pumped on high vacuum for 1 hr to give 20.6 g (104%) of crude 14 that was used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08530593B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-67cd2848cc0b4b2cb1122d1478447e67
출처 메모uspto-grants-2013_09