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HRID 867907作成日:2026年10月25日

Ethanol, 2-chloro-, 1-(4-methylbenzenesulfonate) → 2-(2-Chloroethoxy)benzaldehyde

https://huagongshe.com/reaction/867907

反応式

関与物質

役割名称HCID仕込み量
反応物Ethanol, 2-chloro-, 1-(4-methylbenzenesulfonate)HCID 6639—
反応物SalicylaldehydeHCID 6998—
反応物Potassium CarbonateHCID 11430—
溶媒DimethylformamideHCID 6228—
生成物2-(2-Chloroethoxy)benzaldehydeHCID 384141086%

反応手順

40.0 g of 2- hydroxybenzaldehyde, 84 g of 1-chloro-2-tosyloxyethane and 50 g of potassium carbonate are added to 270 ml of dimethylformamide, and the mixture is stirred at room temperature for 3 days. After the reaction, half of the solvent is distilled off under reduced pressure. About 600 ml of water are added to the residue, and the mixture is extracted with ether. The extract is washed with 10% sodium hydroxide solution and water, dried and then distilled to remove the solvent. The residue is distilled at 116°-118° C./0.2-0.3 mmHg to give 2-(2-chloroethyloxy)benzaldehyde (51.9 g, yield: 86%) as a coloress oil. The properties of this compound are the same as those disclosed in J.O.C., 18, 1380-1402 (1953).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04777178
出典データセットuspto-grants-1988_10
ORD IDord-3477590f4ad34286b63e28571ef0e6ef
出典メモuspto-grants-1988_10