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HRID 442902作成日:2026年10月24日

Water → 3-(Benzyloxy)-5-methylphenol

https://huagongshe.com/ja/reaction/442902

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Benzyl BromideHCID 7498—
反応物Sodium hydrideHCID 24758—
反応物Resorcinol, 5-methyl-, monohydrateHCID 3083941—
溶媒DimethylformamideHCID 6228—
生成物3-(Benzyloxy)-5-methylphenolHCID 1099837932%

反応手順

Orcinol monohydrate (7.10 g, 50 mmol) in N,N-dimethylformamide (20 mL) was added dropwise to NaH (2.4 g, 100 mmol) in N,N-dimethylformamide (60 mL). The reaction mixture was stirred at room temperature for 20 min. Benzyl bromide (8.55 g, 50 mmol) in N,N-dimethylformamide (20 mL) was then added, and the reaction mixture was stirred at ambient temperature for 2 hours. Water (100 mL) was added carefully followed by extraction by ethyl acetate (3×100 mL). The organic phase was washed with brine (2×50 mL), dried over Na2SO4, and concentrated in vacuo. The residue was purified by flash column chromatography (3:1 hexane/ethyl acetate) to give the title compound as a yellow oil (3.40 g, 32%). 1H-NMR (300 MHz, CDCl3) δ 7.39 (m, 5 H), 6.40 (s, 1 H), 6.29 (s, 1 H), 6.26 (s, 1 H), 5.00 (s, 2 H), 4.89 (s, 1 H), 2.26 (s, 3 H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05891909
出典データセットuspto-grants-1999_04
ORD IDord-67ceae663c734f78b75f5827032301ed
出典メモuspto-grants-1999_04