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HRID 41333作成日:2026年10月24日

Formaldehyde → 2-Formyl-6-phenylphenol

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

反応式

関与物質

役割名称HCID仕込み量
反応物FormaldehydeHCID 712—
反応物(1,1'-Biphenyl)-2-olHCID 7017—
反応物TriethylamineHCID 8471—
反応物Magnesium ChlorideHCID 5360315—
溶媒Hydrochloric AcidHCID 313—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物2-Formyl-6-phenylphenolHCID 10703100—

反応条件

温度31.5 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08530593B2
出典データセットuspto-grants-2013_09
ORD IDord-67cd2848cc0b4b2cb1122d1478447e67
出典メモuspto-grants-2013_09