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HRID 11222作成日:2026年10月24日

Cyclopropanecarboxaldehyde → 4-((3,5-Bis(trifluoromethyl)benzyloxy)methyl)-1-(cyclopropylmethyl)-4-phenylazepane

https://huagongshe.com/ja/reaction/11222

反応式

関与物質

役割名称HCID仕込み量
反応物CyclopropanecarboxaldehydeHCID 123114—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物4-((3,5-Bis(trifluoromethyl)benzyloxy)methyl)-4-phenylazepaneHCID 11626160—
触媒Trifluoroacetic acidHCID 6422—
溶媒MethanolHCID 887—
生成物4-((3,5-Bis(trifluoromethyl)benzyloxy)methyl)-1-(cyclopropylmethyl)-4-phenylazepaneHCID 2197311841.5%

反応手順

Mixture of isomer A of 4-((3,5-bis(trifluoromethyl)benzyloxy)methyl)-4-phenylazepane (3 mg) and cyclopropanecarbaldehyde (1.4 mg) in methanol (0.15 mL) was stirred at room temperature for 0.5 hr, then sodium cyanoborohydride (1.0 M solution in THF, 0.02 mL) was added followed by 1 drop of trifluoroacetic acid. The mixture was stirred at room temperature for overnight and concentrated under vacuum. Then saturated sodium bicarbonate and dichloromethane was added to the mixture and the organic layer was separated. The aqueous layer was extracted with dichloromethane 2 times and the combined organic layers were dried over magnesium sulfate, filtered and concentrated under vacuum to give the product as a clear sticky oil (1.4 mg, 41% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07098203B2
出典データセットuspto-grants-2006_08
ORD IDord-55ba5bde656147629274f122dc38c215
出典メモuspto-grants-2006_08