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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7719생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/7719

반응식

참여 물질

역할이름HCID투입량
반응물1,4-DibromobutaneHCID 8056—
반응물Sodium bis(trimethylsilyl)amideHCID 2724254—
반응물[4-(1,3-Benzoxazol-2-yl)-2-chlorophenyl]acetonitrileHCID 10286072—
용매TetrahydrofuranHCID 8028—
생성물1-[4-(1,3-Benzoxazol-2-yl)-2-chlorophenyl]cyclopentanecarbonitrileHCID 10286519—

반응 단계

A solution of [4-(1,3-benzoxazol-2-yl)-2-chlorophenyl]acetonitrile (270 mg, 1.0 mmol) and THF (20 mL) was cooled to −78° C. A solution of NaHMDS (3.7 mL, 2.2 mmol, 0.6M solution in PhMe) was added dropwise via syringe to the reaction. After 15 min at −78° C., 1,4-dibromobutane (143 μL, 1.2 mmol) was added dropwise via syringe. The cooling bath was removed, and the reaction was allowed to warm to rt. The reaction was quenched by the addition of silica gel (600 mg) and concentrated to dryness. The residue was purified by flash chromatography on silica gel (EtOAc:hexanes 1:5) to afford the desired 1-[4-(1,3-benzoxazol-2-yl)-2-chlorophenyl]cyclopentanecarbonitrile as a colorless solid: 1H NMR (CDCl3, 300 MHz) δ 8.34 (s, 1H), 8.12 (dd, 1H), 7.77–7.80 (m, 1H), 7.56–7.62 (m, 2H), 7.35–7.42 (m, 2H), 2.71–2.78 (m, 2H), 2.14–2.26 (m, 2H), 1.89–2.01 (m, 4H). MS (ESI) 323 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087601B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-f11ad2c55b7f49aca6d002758dd0a103
출처 메모uspto-grants-2006_08