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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1175223생성일: 2026년 10월 26일

Cyclohexanol → HCID 59557761, 화합물

https://huagongshe.com/reaction/1175223

반응식

참여 물질

역할이름HCID투입량
반응물CyclohexanolHCID 7966—
반응물Sodium hydrideHCID 24758—
반응물2-(4-(5-Bromo-2-chlorobenzyl)phenoxy)ethyl 4-methylbenzenesulfonateHCID 59557747—
용매TetrahydrofuranHCID 8028—
생성물HCID 59557761HCID 5955776156.6%

반응 조건

온도0 °C

반응 단계

To a solution of cyclohexanol (0.76 g, 7.56 mmol) in anhydrous THF (10 mL), NaH (60%, 0.18 g, 7.56 mmol) was added in portions at 0° C. The mixture was stirred at 0° C. for 0.5 h, and then 2-(4-(5-bromo-2-chlorobenzyl)phenoxy)ethyl 4-methylbenzenesulfonate (intermediate AB) (0.66 g, 1.26 mmol) was added in portions. Then the mixture was stirred at room temperature overnight, whereupon TLC showed the reaction was complete. Then the reaction mixture was quenched with saturated NH4Cl, extracted with EtOAc, washed with water and brine, dried with anhydrous Na2SO4, and concentrated to a crude oil. The crude oil was purified by column chromatography (PE:EA=100:1) to obtain oil AE (0.3 g, yield 56.6%). 1H NMR (400 MHz, CD3OD): δ 7.28-7.21 (m, 3H), 7.07 (d, 2H, J=8.8 Hz), 6.86 (d, 2H, J=8.4 Hz), 4.08 (t, 2H, J=4.8 Hz), 3.98 (s, 2H), 3.80 (t, 2H, J=4.8 Hz), 3.40-3.20 (m, 1H), 1.95-1.93 (m, 2H), 1.76-1.73 (m, 2H), 1.32-1.22 (m, 6H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07838499B2
출처 데이터셋uspto-grants-2010_11
ORD IDord-917a49e89d274d46a662e2b2c3f851e6
출처 메모uspto-grants-2010_11