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HRID 881104作成日:2026年10月26日

Formaldehyde → 2-(4H-benzo[d][1,3]dioxin-6-yl)acetonitrile

https://huagongshe.com/reaction/881104

反応式

関与物質

役割名称HCID仕込み量
反応物FormaldehydeHCID 712—
反応物4-Hydroxybenzyl cyanideHCID 26548—
反応物p-Toluenesulfonic acid monohydrateHCID 521998—
溶媒TolueneHCID 1140—
生成物2-(4H-benzo[d][1,3]dioxin-6-yl)acetonitrileHCID 591662219,757.2%

反応手順

To a solution of (4-hydroxyphenyl)acetonitrile (17.3 g, 0.13 mol) in toluene (350 mL) were added paraformaldehyde (39.0 g, 0.43 mmol) and toluene-4-sulfonic acid monohydrate (2.5 g, 13 mmol) at room temperature. The reaction mixture was heated at reflux for 1 hour. Toluene was removed by evaporation. Water (150 mL) and ethyl acetate (150 mL) were added. The organic layer was separated and the aqueous layer was extracted with ethyl acetate. The combined organics were washed with brine, dried over Na2SO4 and evaporated under vacuum. The residue was separated by preparative HPLC to give 2-(4H-benzo[d][1,3]dioxin-6-yl)acetonitrile (7.35 g, 32%). 1H NMR (400 MHz, CDCl3) δ 7.07-7.11 (m, 1 H), 6.95-6.95 (m, 1 H), 6.88 (d, J=11.6 Hz, 1 H), 5.24 (s, 2 H), 4.89 (s, 2 H), 3.67 (s, 2 H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08993600B2
出典データセットuspto-grants-2015_03
ORD IDord-540a099dc38442f4882dbff502c81059
出典メモuspto-grants-2015_03