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Diethyl Ether → HCID 67958514, 화합물

HRID 527658
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HRID 527658 반응식
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([O:8][CH3:9])[C:3]=1[C:10](=[O:12])[CH3:11].[CH3:13][Mg]Br.CCOCC>C1COCC1>[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([O:8][CH3:9])[C:3]=1[C:10]([OH:12])([CH3:13])[CH3:11]
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참가 물질

5

반응물 3

HCID 3283Diethyl EtherHCID 106786141-(2-Amino-6-methoxyphenyl)ethanoneHCID 178418573HCID 178418573, 화합물

생성물 1

HCID 67958514HCID 67958514, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
0 °C

실험 절차

1-(2-Amino-6-methoxyphenyl)ethanone (500 mg, 3.03 mmol) was dissolved in THF (7.5 mL) and cooled to 0° C. A 3M solution of Methyl magnesium bromide in Et2O (2.12 ml, 6.36 mmol) was added drop wise keeping the temperature below 10° C. The reaction was quenched with an aqueous saturated solution of NH4Cl (7.5 mL) keeping the temperature below 15° C. The mixture was diluted with water and ethyl acetate, two phases separated and the organic layer was washed twice with brine, dried over Na2SO4 and evaporated to dryness affording the title compound (500 mg) as light orange solid.

후처리

  1. customthe temperature below 10° C
  2. customThe reaction was quenched with an aqueous saturated solution of NH4Cl (7.5 mL)
  3. customthe temperature below 15° C
  4. additionThe mixture was diluted with water and ethyl acetate, two phases
  5. customseparated
  6. washthe organic layer was washed twice with brine
  7. dry with materialdried over Na2SO4
  8. customevaporated to dryness

출처 및 근거

ORD 기록
ord-2649a1e0b7f742a4a1934da9c09a57b6
출처 데이터셋
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09346790B2

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