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Water → 4-Carboxymethoxy-3-ethoxyphenylboronic acid

HRID 30752
ノート
印刷プレビュー

反応式

HRID 30752 の反応式
[OH-].[Na+].[CH2:3]([O:5][C:6]1[CH:18]=[C:17]([B:19]2[O:23]C(C)(C)C(C)(C)[O:20]2)[CH:16]=[CH:15][C:7]=1[O:8][CH2:9][C:10]([O:12]CC)=[O:11])[CH3:4].O.C(OCC)(=O)C>C(O)C>[C:10]([CH2:9][O:8][C:7]1[CH:15]=[CH:16][C:17]([B:19]([OH:23])[OH:20])=[CH:18][C:6]=1[O:5][CH2:3][CH3:4])([OH:12])=[O:11]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 962WaterHCID 8857Ethyl AcetateHCID 14798Sodium HydroxideHCID 86605505HCID 86605505、化合物

生成物 1

HCID 231342404-Carboxymethoxy-3-ethoxyphenylboronic acid収率 64.2%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

反応条件

温度
60 °C

実験手順

A 2 mol/L aqueous solution of sodium hydroxide (2.14 mL) was added to a solution of ethyl [2-ethoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy]acetate (0.15 g) in ethanol (10 mL), and the resulting mixture was stirred at 60° C. for 3 hrs. Water and ethyl acetate were added to the reaction mixture. The aqueous layer was separated, washed with ethyl acetate, made acidic with the addition of 2 mol/L hydrochloric acid, and extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to afford the title compound (0.066 g).

後処理

  1. customThe aqueous layer was separated
  2. washwashed with ethyl acetate
  3. additionmade acidic with the addition of 2 mol/L hydrochloric acid
  4. extractionextracted with ethyl acetate
  5. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  6. customThe solvent was evaporated under reduced pressure

出典と根拠

ORDレコード
ord-9432fbf6457d43c09a8ad818b559f197
出典データセット
uspto-grants-2008_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07423185B2

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート