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Phenylboronic Acid → HCID 66915584, 화합물

HRID 449091
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HRID 449091 반응식
[Br:1][C:2]1[C:7]([CH3:8])=[CH:6][C:5]([OH:9])=[C:4]([O:10][CH3:11])[CH:3]=1.[C:12]1(B(O)O)[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1>C(Cl)Cl>[Br:1][C:2]1[CH:3]=[C:4]([O:10][CH3:11])[C:5]([O:9][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[CH:6][C:7]=1[CH3:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 66827Phenylboronic AcidHCID 6123034-Bromo-2-methoxy-5-methylphenol

생성물 1

HCID 66915584HCID 66915584, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

4-Bromo-2-methoxy-5-methylphenol (500 mg, 0.002 mol), phenylboronic acid (0.70 g, 0.0058 mol), TEA (1.9 mL, 0.014 mol), cupric acetate (0.67 g, 0.0037 mol) and DCM (30 mL) were added to a 100 mL oven dried flask and the reaction mixture was stirred at rt for 48 h. Reaction mixture was then filtered through celite. The filtrate was concentrated in vacuo to give a residue which was purified by silica gel chromatography, eluting with 5% EtOAc in hexane. 1H NMR (400 MHz, CDCl3): δ=2.27 (s, 3H), 3.79 (s, 3H), 6.84 (s, 1H), 6.88-6.96 (m, 2H), 7.00-7.08 (m, 1H), 7.15 (s, 1H), 7.23-7.33 (m, 2H).

후처리

  1. customdried flask
  2. customReaction mixture
  3. filtrationwas then filtered through celite
  4. concentrationThe filtrate was concentrated in vacuo
  5. customto give a residue which
  6. customwas purified by silica gel chromatography
  7. washeluting with 5% EtOAc in hexane

출처 및 근거

ORD 기록
ord-7fe76fb624da439aa78e395fe64471bb
출처 데이터셋
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08481733B2

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