Potassium Carbonate → Ethyl 3-[3-tert-butyl-4-(2-{4-[(methylsulfonyl)oxy]phenyl}ethoxy)phenyl]-2-ethoxypropanoate

HRID 353300

反応式

HRID 353300 の反応式
[C:1]([C:5]1[CH:6]=[C:7]([CH2:12][CH:13]([O:19][CH2:20][CH3:21])[C:14]([O:16][CH2:17][CH3:18])=[O:15])[CH:8]=[CH:9][C:10]=1[OH:11])([CH3:4])([CH3:3])[CH3:2].[CH3:22][S:23]([O:26][C:27]1[CH:32]=[CH:31][C:30]([CH2:33][CH2:34]OS(C)(=O)=O)=[CH:29][CH:28]=1)(=[O:25])=[O:24].C(=O)([O-])[O-].[K+].[K+]>CC(=O)CC>[C:1]([C:5]1[CH:6]=[C:7]([CH2:12][CH:13]([O:19][CH2:20][CH3:21])[C:14]([O:16][CH2:17][CH3:18])=[O:15])[CH:8]=[CH:9][C:10]=1[O:11][CH2:34][CH2:33][C:30]1[CH:29]=[CH:28][C:27]([O:26][S:23]([CH3:22])(=[O:24])=[O:25])=[CH:32][CH:31]=1)([CH3:2])([CH3:4])[CH3:3]

参加物

5

実験手順

Ethyl 3-(3-tert-butyl-4-hydroxyphenyl)-2-ethoxypropanoate (0.15 g, 0.44 mmole) and 4-{2-[(methylsulfonyl)oxy]ethyl}phenyl methanesulfonate (0.26 g, 0.89 mmole) were dissolved in 2-butanone (4 ml). Polyethyleneglycol 400 (0.05 g) and anhydrous potassium carbonate (0.092 g, 0.67 mmole) were added the mixture. After stirring at reflux for 16 hours it was checked using HPLC whether all the starting material was consumed. The mixture was washed with water dried with magnesium sulfate and evaporated. Purification of the crude product with preparative HPLC (Kromasil C8, 7 μm, 50×250 mm) using actonitrile(40-80%) in ammonium acetate buffer (pH 7) as mobile phase gave 0.048 g (22% yield) of the desired product

後処理

  1. temperatureat reflux for 16 hours it
  2. customwas consumed
  3. washThe mixture was washed with water
  4. dry with materialdried with magnesium sulfate
  5. customevaporated
  6. customPurification of the crude product with preparative HPLC (Kromasil C8, 7 μm, 50×250 mm)

出典と根拠

ORDレコード
ord-4cada9979f354ec8bfeed55abff49f4d
出典データセット
uspto-grants-2004_06
特許番号
US06750252B2

関連ノート

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