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Potassium Hydroxide → 4-[4-(4-Trifluoromethylphenoxy)phenoxy]-3-hydroxypentanoic acid

HRID 638509
ノート
印刷プレビュー

反応式

HRID 638509 の反応式
[F:1][C:2]([F:28])([F:27])[C:3]1[CH:26]=[CH:25][C:6]([O:7][C:8]2[CH:24]=[CH:23][C:11]([O:12][CH:13]([CH3:22])[CH:14]([OH:21])[CH2:15][C:16]([O:18]CC)=[O:17])=[CH:10][CH:9]=2)=[CH:5][CH:4]=1.[OH-].[K+].OC(CC)CC(O)=O>CO>[F:1][C:2]([F:27])([F:28])[C:3]1[CH:4]=[CH:5][C:6]([O:7][C:8]2[CH:24]=[CH:23][C:11]([O:12][CH:13]([CH3:22])[CH:14]([OH:21])[CH2:15][C:16]([OH:18])=[O:17])=[CH:10][CH:9]=2)=[CH:25][CH:26]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 14797Potassium HydroxideHCID 1078023-Hydroxyvaleric acidHCID 12856783Ethyl 4-[4-(4-trifluoromethylphenoxy)phenoxy]-3-hydroxypentanoate

生成物 1

HCID 128567844-[4-(4-Trifluoromethylphenoxy)phenoxy]-3-hydroxypentanoic acid

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

A mixture of 7.0 g of ethyl 4-[4-(4-trifluoromethylphenoxy)phenoxy]-3-hydroxypentanoate and 1.74 g of 85% KOH in 30 ml ag. methanol was stirred at room temperature for 1.5 hrs. The mixture was concentrated, poured into water and acidified. The product was dissolved in ether, washed with brine, dried over MgSO4 and vacuum evaporated to yield 6.0 of product which was identified as the subject 3-hydroxypentanoic acid.

後処理

  1. concentrationThe mixture was concentrated
  2. additionpoured into water
  3. dissolutionThe product was dissolved in ether
  4. washwashed with brine
  5. dry with materialdried over MgSO4 and vacuum
  6. customevaporated
  7. customto yield 6.0 of product which

出典と根拠

ORDレコード
ord-471c0fe6e02444de82f2b5a29d2ee678
出典データセット
uspto-grants-1985_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04561882

反応ノート

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