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HRID 7734생성일: 2026년 10월 23일

1,4-Dibromobutane → 1-[4-(1,3-Benzoxazol-2-yl)-2-methoxyphenyl]cyclopentanecarbonitrile

https://huagongshe.com/ko/reaction/7734

반응식

참여 물질

역할이름HCID투입량
반응물1,4-DibromobutaneHCID 8056—
반응물Sodium bis(trimethylsilyl)amideHCID 2724254—
반응물BomaHCID 10192854—
용매TetrahydrofuranHCID 8028—
생성물1-[4-(1,3-Benzoxazol-2-yl)-2-methoxyphenyl]cyclopentanecarbonitrileHCID 10236667—

반응 단계

[4-(1,3-Benzoxazol-2-yl)-2-methoxyphenyl]acetonitrile (130 mg, 0.49 mmol) in THF (5.0 mL) was cooled to −78° C. under argon atmosphere. Sodium bis(trimethylsilyl)amide (1.8 mL, 1.08 mmol) was added slowly and after fifteen minutes, added 1,4-dibromobutane (0.07 mL, 0.59 mmol) to dark brown reaction mixture. Let mixture warm to rt overnight. After concentrating reaction mixture in vacuo, the resulting pink oil was purified by flash chromatography, using a gradient elution of 1:9 EtOAc:hexanes to 1:4 EtOAc:hexanes. This afforded the desired compound, 1-[4-(1,3-benzoxazol-2-yl)-2-methoxyphenyl]cyclopentanecarbonitrile, as a yellow solid. 1H NMR(CDCl3, 300 MHz) δ 7.86–7.26 (m, 7H), 4.07 (s, 3H), 2.59–1.91 (m, 8H). MS (ESI) 319.1 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087601B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-34ed716cd4364862b6fb3902c6311fb6
출처 메모uspto-grants-2006_08