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Potassium Hydroxide → 4-(2-Chloroethoxy)benzoic acid

HRID 354067
ノート
印刷プレビュー

反応式

HRID 354067 の反応式
C[C:2]1[CH:10]=[C:9]([O:11][CH2:12][CH2:13][Cl:14])[CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].[OH-].[K+]>CO>[Cl:14][CH2:13][CH2:12][O:11][C:9]1[CH:10]=[CH:2][C:3]([C:4]([OH:6])=[O:5])=[CH:7][CH:8]=1
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

4

反応物 2

HCID 14797Potassium HydroxideHCID 23512918methyl 4-(2-Chloroethoxy)-benzoic acid

生成物 1

HCID 123892684-(2-Chloroethoxy)benzoic acid収率 93.2%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
50 °C

実験手順

To methyl 4-(2-Chloroethoxy)-benzoic acid (11.8 gm, 53.5 mmol) dissolved in 118 mL of methanol was added 2N KOH (35mL, 1.3 equiv.) and the resulting solution was heated at 50° C. for 24 hrs. The reaction was cooled to room temperature and the methanol evaporated off. The residue was diluted with water and extracted once with ethyl acetate. The aqueous layer was then acidified with 6N HCl and a precipitate formed which was filtered off, washed well with water, and pumped dry under vacuum to yield 10 gm of the title compound.

後処理

  1. temperatureThe reaction was cooled to room temperature
  2. customthe methanol evaporated off
  3. additionThe residue was diluted with water
  4. extractionextracted once with ethyl acetate
  5. customa precipitate formed which
  6. filtrationwas filtered off
  7. washwashed well with water
  8. custompumped dry under vacuum

出典と根拠

ORDレコード
ord-d7372df631b542349a22e590570c18c4
出典データセット
uspto-grants-2004_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06756388B1

反応ノート

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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