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Water → HCID 67546464, 화합물

HRID 2251837
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HRID 2251837 반응식
[CH3:1][C:2]([C:6]1[CH:11]=[CH:10][C:9]([N+:12]([O-:14])=[O:13])=[CH:8][CH:7]=1)([CH3:5])[CH2:3][OH:4].[H-].[Na+].[CH3:17]I.O>C1COCC1>[CH3:17][O:4][CH2:3][C:2]([C:6]1[CH:11]=[CH:10][C:9]([N+:12]([O-:14])=[O:13])=[CH:8][CH:7]=1)([CH3:1])[CH3:5]
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6

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HCID 962WaterHCID 6328Methyl iodideHCID 24758Sodium hydrideHCID 222492792-Methyl-2-(4-nitrophenyl)propan-1-ol

생성물 1

HCID 67546464HCID 67546464, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
0 °C

실험 절차

To a stirred solution of 2-methyl-2-(4-nitro-phenyl)-propan-1-ol (prepared by the method described in WO02/66470) (200 mg, 1 mmol) in THF (15 mL) was added NaH (43 mg, 60% in oil) at 0° C. The mixture was stirred at 0° C. for 20 min, MeI (0.22 mL, 1.5 mmol) was added and the mixture was stirred for 2 h at 0° C. then overnight at RT. H2O was added and the mixture was extracted with EtOAc. The organic phase was dried, filtered and evaporated to give 1-(2-methoxy-1,1-dimethyl-ethyl)-4-nitro-benzene.

후처리

  1. stirringthe mixture was stirred for 2 h at 0° C.
  2. customovernight
  3. customat RT
  4. extractionthe mixture was extracted with EtOAc
  5. customThe organic phase was dried
  6. filtrationfiltered
  7. customevaporated

출처 및 근거

ORD 기록
ord-7a35f7e0a3f247b2a64f8c7aab5c0a0c
출처 데이터셋
uspto-grants-2008_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07320992B2

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