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

HRID 2164837
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인쇄 미리보기

반응식

HRID 2164837 반응식
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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 5

HCID 313Hydrochloric AcidHCID 962WaterHCID 5234Sodium ChlorideHCID 14797Potassium HydroxideHCID 70490311HCID 70490311, 화합물

생성물 1

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

시약·촉매·용매 1

HCID 174
Ethylene Glycol
용매

실험 절차

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°).

후처리

  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

출처 및 근거

ORD 기록
ord-89d9d91ff9d54ce79042e2a45dec559d
출처 데이터셋
uspto-grants-1985_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04507317

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