Dimethylformamide → 3-(3-Methoxyphenyl)-3-methylbutanoic acid

HRID 1662557ノート

反応式

HRID 1662557 の反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:9]([CH:12]2C(=O)OC(C)(C)[O:14][C:13]2=[O:21])([CH3:11])[CH3:10])[CH:6]=[CH:7][CH:8]=1.CN(C=O)C>O>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:9]([CH3:11])([CH3:10])[CH2:12][C:13]([OH:21])=[O:14])[CH:6]=[CH:7][CH:8]=1

参加物

4

反応条件

温度
100 °C

実験手順

The 5-(2-(3-methoxyphenyl)propan-2-yl)-2,2-dimethyl-1,3-dioxane-4,6-dione 85.C (0.313 g, 1.1 mmol) was dissolved in DMF (1.50 mL, 19 mmol). To the solution was added water (0.15 mL, 8.3 mmol). The resulting solution was then heated to 100° C. and stirred for four hours. The reaction was cooled to room temperature and then diluted with water. The mixture was extracted with EtOAc (2×50 mL). The combined organic layers were then washed with 1N lithium chloride solution (1×20 mL) and brine (1×20 mL) and dried over magnesium sulfate. The filtrate was then concentrated to give crude 3-(3-methoxyphenyl)-3-methylbutanoic acid 85.D (0.247 g, 111% yield) that was used directly in the following reaction. MS ESI (pos.) m/e: 226.1 (M+H2O)+.

後処理

  1. temperatureThe reaction was cooled to room temperature
  2. extractionThe mixture was extracted with EtOAc (2×50 mL)
  3. washThe combined organic layers were then washed with 1N lithium chloride solution (1×20 mL) and brine (1×20 mL)
  4. dry with materialdried over magnesium sulfate
  5. concentrationThe filtrate was then concentrated

出典と根拠

ORDレコード
ord-d87253ef0b0249d2b0a373d301e70704
出典データセット
uspto-grants-2011_10
特許番号
US08030354B2

反応ノート

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