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Hydrochloric Acid → 4-(3-Chloro[1,1'-biphenyl]-2-yl)butanoic acid

HRID 2164837
ノート
印刷プレビュー

反応式

HRID 2164837 の反応式
Cl[C:2]1([CH2:14][CH2:15][CH2:16][C:17]#N)[CH2:7][CH:6]=[CH:5][CH:4]=[C:3]1[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1.[OH-:19].[K+].[ClH:21].[Cl-].[Na+].[OH2:24]>C(O)CO>[Cl:21][C:7]1[C:2]([CH2:14][CH2:15][CH2:16][C:17]([OH:24])=[O:19])=[C:3]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH:4]=[CH:5][CH:6]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 5

HCID 313Hydrochloric AcidHCID 962WaterHCID 5234Sodium ChlorideHCID 14797Potassium HydroxideHCID 70490311HCID 70490311、化合物

生成物 1

HCID 132813484-(3-Chloro[1,1'-biphenyl]-2-yl)butanoic acid

試薬・触媒・溶媒 1

HCID 174
Ethylene Glycol
溶媒

実験手順

A stirred solution of 4-(2-chloro[1,1'-biphenyl]-2-yl)butanenitrile (2.7 g, 0.011 mole), potassium hydroxide (6.9 g, 0.11 mole), and ethylene glycol (25 ml) in water (25 ml) was heated at reflux for approximately 18 hours. The reaction mixture was cooled to room temperature, diluted with ice water (100 g) and acidified with concentrated hydrochloric acid. The mixture was saturated with sodium chloride, then extracted with diethyl ether (three 100 ml portions) and methylene chloride (100 ml). The extracts were combined, dried over anhydrous magnesium sulfate, filtered and the filtrate evaporated under reduced pressure to yield 4-(3-chloro[1,1'-biphenyl]-2-yl)butanoic acid as a solid (m.p. 74°-76°).

後処理

  1. temperatureat reflux for approximately 18 hours
  2. extractionextracted with diethyl ether (three 100 ml portions) and methylene chloride (100 ml)
  3. dry with materialdried over anhydrous magnesium sulfate
  4. filtrationfiltered
  5. customthe filtrate evaporated under reduced pressure

出典と根拠

ORDレコード
ord-89d9d91ff9d54ce79042e2a45dec559d
出典データセット
uspto-grants-1985_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04507317

反応ノート

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