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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 11222생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물CyclopropanecarboxaldehydeHCID 123114—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물4-((3,5-Bis(trifluoromethyl)benzyloxy)methyl)-4-phenylazepaneHCID 11626160—
촉매Trifluoroacetic acidHCID 6422—
용매MethanolHCID 887—
생성물4-((3,5-Bis(trifluoromethyl)benzyloxy)methyl)-1-(cyclopropylmethyl)-4-phenylazepaneHCID 2197311841.5%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07098203B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-55ba5bde656147629274f122dc38c215
출처 메모uspto-grants-2006_08