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Methanol → 5-Hydroxy-[1,1'-biphenyl]-2-carbaldehyde

HRID 445832
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HRID 445832 반응식
Br[C:2]1[CH:9]=[C:8]([OH:10])[CH:7]=[CH:6][C:3]=1[CH:4]=[O:5].[C:11]1(B(O)O)[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1.C(=O)(O)[O-].[Na+].CO>C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.O.C(OCC)(=O)C.C1(C)C=CC=CC=1>[OH:10][C:8]1[CH:9]=[C:2]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[C:3]([CH:4]=[O:5])=[CH:6][CH:7]=1
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참가 물질

9

반응물 4

HCID 887MethanolHCID 66827Phenylboronic AcidHCID 516892Sodium BicarbonateHCID 110848662-Bromo-4-hydroxybenzaldehyde

생성물 1

HCID 573034645-Hydroxy-[1,1'-biphenyl]-2-carbaldehyde

시약·촉매·용매 4

HCID 178418397HCID 178418397, 화합물
촉매
HCID 962Water용매
HCID 1140Toluene용매
HCID 8857Ethyl Acetate용매

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온도
120 °C

실험 절차

A mixture of 2-bromo-4-hydroxybenzaldehyde (350 mg, 1.74 mmol), phenyl boronic acid (233.5 mg, 1.92 mmol), Pd(PPh3)4 (60 mg, 0.052 mmol), saturated sodium bicarbonate (6.0 mL), methanol (15 mL), and toluene (6.0 mL) was heated in a pressure tube at 120° C. overnight. Ethyl acetate and water were added and the layers separated. The aqueous phase was extracted with ethyl acetate and the combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo. The crude compound was purified by flash column chromatography on silica gel with hexanes and EtOAc (30%) to afford 5-hydroxy-[1,1′-biphenyl]-2-carbaldehyde (651).

후처리

  1. customthe layers separated
  2. extractionThe aqueous phase was extracted with ethyl acetate
  3. dry with materialthe combined organic layers were dried over sodium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo
  6. customThe crude compound was purified by flash column chromatography on silica gel with hexanes and EtOAc (30%)

출처 및 근거

ORD 기록
ord-95808328835545a5bc47789b00b2f2db
출처 데이터셋
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08476308B2

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