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Citric Acid → 4-Fluoro-5-iodo-2-methoxyphenol

HRID 1438134
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HRID 1438134 반응식
C([O:4][C:5]1[CH:10]=[C:9]([I:11])[C:8]([F:12])=[CH:7][C:6]=1[O:13][CH3:14])(=O)C.[OH-].[Na+].C(O)(=O)CC(CC(O)=O)(C(O)=O)O>C1COCC1.CO>[F:12][C:8]1[C:9]([I:11])=[CH:10][C:5]([OH:4])=[C:6]([O:13][CH3:14])[CH:7]=1
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참가 물질

6

반응물 3

HCID 311Citric AcidHCID 14798Sodium HydroxideHCID 59838025HCID 59838025, 화합물

생성물 1

HCID 598380024-Fluoro-5-iodo-2-methoxyphenol수율 100%

시약·촉매·용매 2

HCID 887Methanol용매HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of 64B (680 mg, 2.19 mmol) in THF (3.0 mL) and MeOH (1.0 mL) was added 1.0 N NaOH (2.74 mL, 2.74 mmol). The reaction was stirred at rt for 2.0 h before it was acidified by addition of 5% citric acid. The mixture was extracted with EtOAc, washed with brine and dried over Na2SO4. After evaporation of the solvent, 64C (586 mg, 100% yield) was obtained as a solid and used for next step without further purification. 1H NMR (400 MHz, CDCl3) δ ppm 3.85 (s, 3H) 6.62 (d, J=8.79 Hz, 1H) 7.21 (d, J=6.15 Hz, 1H).

후처리

  1. extractionThe mixture was extracted with EtOAc
  2. washwashed with brine
  3. dry with materialdried over Na2SO4
  4. customAfter evaporation of the solvent

출처 및 근거

ORD 기록
ord-79e9f5ccd88e4338a7588162735ddf5c
출처 데이터셋
uspto-grants-2009_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07622585B2

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