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HRID 424288作成日:2026年10月25日

Acetic Acid → 1-Nitro-2-phenylethane

https://huagongshe.com/reaction/424288

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物Beta-NitrostyreneHCID 7626—
反応物Sodium borohydrideHCID 4311764—
溶媒1,4-DioxaneHCID 31275—
溶媒Dioxan ethanolHCID 22560076—
生成物1-Nitro-2-phenylethaneHCID 8020883%

反応手順

In a 500 mL two-necked flask equipped with a thermometer and a pressure-equalizing dropping funnel, NaBH4 (5.33 g, 0.140 mol) was suspended in 1,4-dioxane/ethanol (100 mL/30 ml). ≈-Nitrostyrene (3, 10.0 g, 67.0 mmol) in 1,4-dioxane (100 mL) was added dropwise to the solution over 45 minutes, keeping the temperature below 30° C. A fine slurry formed during the addition. After the addition the reaction mixture was stirred overnight, then ice/water (125 mL) was added, and a 50% solution of acetic acid was added to neutralize excess NaBH4; the clear solution was then concentrated in vacuo and the residue was dissolved in water and extracted twice with CH2Cl2. The organic phase was washed with water (2×30 mL) and brine (1×30 mL), dried (Na2SO4), filtered and evaporated in vacuo obtaining 4 (8.40 g, 83%) as yellow oil. ESI-MS: 152 (MH+) (Calc. for C8H9NO2: 151).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08105567B2
出典データセットuspto-grants-2012_01
ORD IDord-360d644d2bd343edab5d583f6ce741f3
出典メモuspto-grants-2012_01