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HRID 3001作成日:2026年10月26日

Dihydrobenzofuran → 2,3-Dihydrobenzofuran-5-carboxaldehyde

https://huagongshe.com/reaction/3001

反応式

関与物質

役割名称HCID仕込み量
反応物DihydrobenzofuranHCID 10329—
反応物Methane, dichloromethoxy-HCID 21004—
溶媒Diethyl EtherHCID 3283—
溶媒DichloromethaneHCID 6344—
生成物2,3-Dihydrobenzofuran-5-carboxaldehydeHCID 73590160.3%

反応条件

温度0 °C

反応手順

To a stirred solution of α,α-dichloromethyl methyl ether (2.15 g, 19 mmol, 1.35 eq) in methylene chloride (30 mL) at -40° C. was added successively stannic chloride (1.65 g, 17 mmol, 1.2 eq) and 15 minutes later, a solution of 2,3-dihydrobenzofuran (1.68 g, 14 mmol) in CH2Cl2 (5 mL) maintaining the temperature at or below -35° C. The mixture was warmed to 0° C., stirred 1 hour, then poured into ice-water, and stirred a further 30 minutes. The mixture was diluted with ether, and the phases separated. The organic phase was concentrated in vacuo, and the residue purified by vacuum distillation to yield the title compound (1.25 g, 60%) as a colorless liquid. b.p. 119°-121° C. at 0.3 mm Hg.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05731434
出典データセットuspto-grants-1998_03
ORD IDord-a77e34e2ec91434fa697b43c33d45133
出典メモuspto-grants-1998_03