Isopropanol → 6-(3-Methoxyphenyl)-4-Propylmorpholin-3-one

HRID 2102341ノート

反応式

HRID 2102341 の反応式
[OH-].[K+].C(O)(C)C.Cl[CH2:8][C:9]([N:11]([CH2:15][CH:16]([OH:25])[C:17]1[CH:22]=[CH:21][CH:20]=[C:19]([O:23][CH3:24])[CH:18]=1)[CH2:12][CH2:13][CH3:14])=[O:10]>O>[CH3:24][O:23][C:19]1[CH:18]=[C:17]([CH:16]2[CH2:15][N:11]([CH2:12][CH2:13][CH3:14])[C:9](=[O:10])[CH2:8][O:25]2)[CH:22]=[CH:21][CH:20]=1

参加物

5

反応物 3

HCID 3776IsopropanolHCID 14797Potassium HydroxideHCID 574406812-Chloro-N-[2-hydroxy-2-(3-methoxyphenyl)ethyl]-N-propylacetamide

生成物 1

HCID 150064786-(3-Methoxyphenyl)-4-Propylmorpholin-3-one収率 100%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

Potassium hydroxide (4.2 g, 0.07 mol), isopropyl alcohol (500 ml) and the amide from example 4 (17.8 g, 0.06 mol) were stirred together as an opaque solution with water (15 ml) for 2 hours. The reaction mixture was concentrated in vacuo and the yellow residue dissolved in ethyl acetate (200 ml. This was partitioned with water (200 ml) then brine (200 ml). The organic fraction was dried over anhydrous magnesium sulphate, filtered and concentrated in vacuo to give the title compound as a yellow oil (15.8 g, 0.06 mol, 100%). 1H NMR (CDCl3, 400 MHz) δ: 0.96 (t, 3H), 1.62 (m, 2H), 3.36 (m, 2H), 3.51 (q, 2H), 3.81 (s, 3H), 4.30-4.62 (bq, 2H), 4.79 (d, 1H), 6.85 (d, 1H), 6.91 (d, 1H), 6.95 (s, 1H), 7.29 (t, 1H). LRMS: m/z 272. Analysis found C, 66.80; H, 7.78; N, 5.52%. C14H19NO3.0.1H2O requires C, 66.96; H, 7.71; N, 5.58%.

後処理

  1. concentrationThe reaction mixture was concentrated in vacuo
  2. dissolutionthe yellow residue dissolved in ethyl acetate (200 ml
  3. customThis was partitioned with water (200 ml)
  4. dry with materialThe organic fraction was dried over anhydrous magnesium sulphate
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-6922ce224daf4d919422a453cbb12fa3
出典データセット
uspto-grants-2009_08
特許番号
US07576081B2

反応ノート

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