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HRID 59775作成日:2026年10月25日

3-Furancarboxaldehyde, tetrahydro- → HCID 178424141、化合物

https://huagongshe.com/reaction/59775

反応式

関与物質

役割名称HCID仕込み量
反応物3-Furancarboxaldehyde, tetrahydro-HCID 157568—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物HCID 178424139HCID 178424139—
溶媒Acetic AcidHCID 176—
溶媒MethanolHCID 887—
溶媒Sodium BicarbonateHCID 516892—
生成物HCID 178424141HCID 178424141—
生成物HCID 178424142HCID 178424142—

反応手順

To a solution of 61 mg trans-4-(2-o-tolyl-chroman-6-yloxy)-cyclohexylamine (0.18 mmol) in 3 ml methanol and 0.2 ml of acetic acid at room temperature 39 mg tetrahydrofuran-3-carboxaldehyde (0.20 mmol) in 3 ml of methanol were added, and 12 mg of sodium cyanoborohydride (0.89 mmol (0.20 mmol) were then added in one portion. Stirring at room temperature was continued for 16 h. The solution was diluted with aqueous saturated sodium hydrogencarbonate solution and the aqueous layer extracted with dichloromethane. The combined organic layers were dried with sodium sulfate and filtered, and the solvent removed under reduced pressure. The crude product was purified by RP-HPLC. 23 mg of (tetrahydrofuran-3-ylmethyl)-[trans-4-(2-o-tolyl-chroman-6-yloxy)-cyclohexyl]-amine and 19 mg of bis-(tetrahydrofuran-3-ylmethyl)-[trans-4-(2-o-tolyl-chroman-6-yloxy)-cyclohexyl]-amine were isolated.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09440941B2
出典データセットuspto-grants-2016_09
ORD IDord-49890fe6d6d0441ab752901cbf80fecd
出典メモuspto-grants-2016_09