Lithium hydroxide, monohydrate → 3-{4-[2-(4-tert-Butoxycarbonylaminophenyl)ethoxy]phenyl}-2-ethoxypropanoic acid

HRID 1375714ノート

反応式

HRID 1375714 の反応式
O.[OH-].[Li+].C([O:6][C:7](=[O:36])[CH:8]([O:33][CH2:34][CH3:35])[CH2:9][C:10]1[CH:15]=[CH:14][C:13]([O:16][CH2:17][CH2:18][C:19]2[CH:24]=[CH:23][C:22]([NH:25][C:26]([O:28][C:29]([CH3:32])([CH3:31])[CH3:30])=[O:27])=[CH:21][CH:20]=2)=[CH:12][CH:11]=1)C>O.O1CCCC1>[C:29]([O:28][C:26]([NH:25][C:22]1[CH:21]=[CH:20][C:19]([CH2:18][CH2:17][O:16][C:13]2[CH:12]=[CH:11][C:10]([CH2:9][CH:8]([O:33][CH2:34][CH3:35])[C:7]([OH:36])=[O:6])=[CH:15][CH:14]=2)=[CH:24][CH:23]=1)=[O:27])([CH3:32])([CH3:31])[CH3:30]

参加物

5

実験手順

Lithium hydroxide hydrate (77 mg; 1.85 mmole) in water (5.5 ml) was slowly added to a solution of 3-{4-[2-(4-tert-butoxycarbonylaminophenyl)ethoxy]phenyl}-2-ethoxypropanoic acid ethyl ester (0.77 g; 1.68 mmole) in tetrahydrofuran (7.6 ml). After stirring at room temperature for 4 hours the reaction mixture was kept in a freezer for 4 days. Tetrahydrofuran was removed by evaporation in vacuo. More water was added and the mixture was acidified with hydrochloric acid to pH 1. The product was extracted with ethyl acetate, washed twice with water, dried (sodium sulfate), filtered and the solvent was evaporated in vacuo to give 0.716 g of 3-{4-[2-(4-tert-butoxycarbonylaminophenyl)-ethoxy]phenyl}-2-ethoxypropanoic acid.

後処理

  1. waitwas kept in a freezer for 4 days
  2. customTetrahydrofuran was removed by evaporation in vacuo
  3. additionMore water was added
  4. extractionThe product was extracted with ethyl acetate
  5. washwashed twice with water
  6. dry with materialdried (sodium sulfate)
  7. filtrationfiltered
  8. customthe solvent was evaporated in vacuo

出典と根拠

ORDレコード
ord-a52c49261e4f4ce9b99e025544c98c96
出典データセット
uspto-grants-2007_01
特許番号
US07169810B2

反応ノート

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