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Diethyl Ether → HCID 67958514、化合物

HRID 527658
ノート
印刷プレビュー

反応式

HRID 527658 の反応式
[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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 3283Diethyl EtherHCID 106786141-(2-Amino-6-methoxyphenyl)ethanoneHCID 178418573HCID 178418573、化合物

生成物 1

HCID 67958514HCID 67958514、化合物

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
0 °C

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-2649a1e0b7f742a4a1934da9c09a57b6
出典データセット
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09346790B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート