참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Reserpine | HCID 5770 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 4-Bromo-2-chlorophenol | HCID 19859 | — |
| 반응물 | Phenylboronic Acid | HCID 66827 | — |
| 촉매 | Cupric acetate | HCID 8895 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | Heptane | HCID 8900 | — |
| 생성물 | 4-Bromo-2-chloro-1-phenoxybenzene | HCID 22736309 | — |
반응 단계
A mixture of 4-bromo-2-chlorophenol (2.07 g, 10 mmol), phenyl boronic acid (3.66 g, 30 mmol), copper(II) acetate (2.0 g, 1.1 mmol) and 4A powdered molecular sieves (20 g) in dichloromethane (100 mL) was treated with triethylamine (5.0 g, 50 mmol) then stirred at ambient temperature for 5 days. The mixture was diluted with heptane (100 mL), then filtered through a bed of celite. The filtrate was concentrated under reduced pressure to remove dichloromethane. The mixture was extracted with IN hydrochloric acid, 15 wt % aqueous sodium hydroxide, brine and then dried over magnesium sulfate. The mixture was filtered and the filtrate concentrated under reduced pressure to provide (1.27 g, 45%): 1H NMR (DMSO-d6, 400 MHz) δ 7.87(s, 1H), 7.55(d, 1H), 7.40(t, 2H), 7.17(t, 1H), 6.99(m, 3H); MS MH+283; RP-HPLC (Hypersil HS, 5 μm, 100 A 4.6×250 mm; 25%-100% acetonitrile—0.05 M ammonium acetate over 10 min, 1 m/min) tr 14.42min.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06713474B2 |
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| 출처 데이터셋 | uspto-grants-2004_03 |
|---|
| ORD ID | ord-11c4d1aba29d43eb826cea2fa995c699 |
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| 출처 메모 | uspto-grants-2004_03 |
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