Potassium Carbonate → 1-(3-Amino-4-hydroxyphenyl)ethanone O-methyloxime

HRID 1968999ノート

反応式

HRID 1968999 の反応式
Cl.[CH3:2][O:3][NH2:4].[NH2:5][C:6]1[CH:11]=[C:10]([C:12]2([CH3:17])OCCO2)[CH:9]=[CH:8][C:7]=1[OH:18].C(=O)([O-])[O-].[K+].[K+]>C(O)C>[CH3:2][O:3][N:4]=[C:12]([C:10]1[CH:9]=[CH:8][C:7]([OH:18])=[C:6]([NH2:5])[CH:11]=1)[CH3:17]

参加物

5

反応物 3

HCID 11430Potassium CarbonateHCID 521874O-Methylhydroxylamine hydrochlorideHCID 59444173HCID 59444173、化合物

生成物 1

HCID 1363371921-(3-Amino-4-hydroxyphenyl)ethanone O-methyloxime

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

A mixture of O-methylhydroxylamine hydrochloride (535 mg, 6.40 mmol), 2-amino-4-(2-methyl-1,3-dioxolan-2-yl)phenol D130 (250 mg, 1.28 mmol) and potassium carbonate (442 mg, 3.20 mmol) in ethanol (10 mL) was heated to reflux for 2 hr. The mixture was cooled to rt and concentrated to dryness under vacuum and the residue partitioned between DCM and water. The organic phase was separated washed with brine, dried (MgSO4) and concentrated to dryness in vacuo. The residue was purified using silica gel chromatography eluting with 0 to 10% MeOH in DCM. The title product was isolated as a pale brown solid, 224 mg, 97%.

後処理

  1. temperaturewas heated
  2. temperatureto reflux for 2 hr
  3. concentrationconcentrated to dryness under vacuum
  4. customthe residue partitioned between DCM and water
  5. customThe organic phase was separated
  6. washwashed with brine
  7. dry with materialdried (MgSO4)
  8. concentrationconcentrated to dryness in vacuo
  9. customThe residue was purified
  10. washeluting with 0 to 10% MeOH in DCM

出典と根拠

ORDレコード
ord-16c33f0d5ce6487186a8cd44d8b455ac
出典データセット
uspto-grants-2013_04
特許番号
US08426443B2

反応ノート

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