2,5-Dichlorobenzoic acid → 3-Chloro-6-(3,5-diisopropylphenoxy)benzoic Acid

HRID 1733405

반응식

HRID 1733405 반응식
Cl[C:2]1[CH:10]=[CH:9][C:8]([Cl:11])=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].[CH:12]([C:15]1[CH:16]=[C:17]([OH:24])[CH:18]=[C:19]([CH:21]([CH3:23])[CH3:22])[CH:20]=1)([CH3:14])[CH3:13].[H-].[Na+]>C1(C)C(C)=CC=CC=1>[Cl:11][C:8]1[CH:7]=[C:3]([C:2]([O:24][C:17]2[CH:18]=[C:19]([CH:21]([CH3:22])[CH3:23])[CH:20]=[C:15]([CH:12]([CH3:14])[CH3:13])[CH:16]=2)=[CH:10][CH:9]=1)[C:4]([OH:6])=[O:5]

참가 물질

5

반응물 3

HCID 57842,5-Dichlorobenzoic acidHCID 24758Sodium hydrideHCID 931043,5-Bis(1-methylethyl)phenol

생성물 1

HCID 202989673-Chloro-6-(3,5-diisopropylphenoxy)benzoic Acid수율 49.4%

시약·촉매·용매 1

HCID 7237O-Xylene용매

실험 절차

2,5-dichlorobenzoic acid (5 g) and 3,5-diisopropylphenol (4.66 g) were dissolved in dry xylene and the solution placed under dry oxygen-free nitrogen. Sodium hydride (1.25 g) was added as a suspension in petroleum ether. Cuprous bromide was added and the solution refluxed for 5 hours and cooled. The xylene was removed by low pressure distillation. The remaining solid was acidified with dilute hydrochloric acid and extracted with diethyl ether. The ethereal layer was separated, dried and distilled under low pressure to give an oil. The oil was dissolved in petroleum ether (30°-40° ). Standing gave a crystalline solid, which was recrystallised from hexane to give the title compound (4.3 g), mp 129°-130° C.

후처리

  1. temperaturethe solution refluxed for 5 hours
  2. temperaturecooled
  3. customThe xylene was removed by low pressure distillation
  4. extractionextracted with diethyl ether
  5. customThe ethereal layer was separated
  6. customdried
  7. distillationdistilled under low pressure
  8. customto give an oil
  9. customStanding gave a crystalline solid, which
  10. customwas recrystallised from hexane

출처 및 근거

ORD 기록
ord-c41674c889ed47979e95692495323db8
출처 데이터셋
uspto-grants-1980_12
특허 번호
US04242121

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