تفاعل #6694

ord-6ad8b409962b46c38cd36eb904e5406a

معادلة التفاعل

CCCCCOCCCCOc1ccc(B(O)O)c(F)c1F
2,3-difluoro-4-(4-pentyloxybutoxy)phenylboronic acid
CCCCCOCCCCOc1ccc(B(O)O)c(F)c1F
2,3-Difluoro4-(4-pentyloxybutoxy)phenylboronic acid
O=C(O)c1ccc(OCc2ccccc2)cc1
4-bromo-benzoic acid ethyl ester
O=C(O)c1ccc(OCc2ccccc2)cc1
4-Benzyloxybenzoic acid
O=C([O-])[O-].[Na+].[Na+]
sodium carbonate
CCCCCOCCCCOc1ccc(-c2ccc(C(=O)OCC)cc2)c(F)c1F
2′,3′-difluoro-4′-(4-pentyloxybutoxy)-biphenyl-4-carboxylic acid ethyl ester
المردود 88.0%
CCCCCOCCCCOc1ccc(-c2ccc(C(=O)OCC)cc2)c(F)c1F
2′,3′-Difluoro-4′-(4-pentyloxybutoxy)-biphenyl-4-carboxylic acid ethyl ester
المردود 88.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    استخلاصextracted with ethyl acetate:hexane(1:1)
  2. 2
    غسيلwashed with brine
  3. 3
    تجفيفdried over MgSO4
  4. 4
    تركيزconcentrated in vacuo
  5. 5
    أخرىThe purification by chromatography
  6. 6
    أخرىon silica gel (5% EtOAc/hexanes) and recrystallization from acetonitrile

الإجراء التجريبي

A biphasic solution of 2,3-difluoro-4-(4-pentyloxybutoxy)phenylboronic acid (25) (1 equi.), 4-bromo-benzoic acid ethyl ester (12), (1 equi.), sodium carbonate (2.7 equi.), and tetrakis(triphenylphoshine)palladium catalyst (0.01 equi.) in water-toluene (1:1) (2 mL/mmole) was stirred at 100 C. temperature for 12 h., cooled to room temperature, extracted with ethyl acetate:hexane(1:1), washed with brine, dried over MgSO4, and concentrated in vacuo. The purification by chromatography on silica gel (5% EtOAc/hexanes) and recrystallization from acetonitrile afforded 2′,3′-difluoro-4′-(4-pentyloxybutoxy)-biphenyl-4-carboxylic acid ethyl ester (26) as a white solid (88%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07083832B2uspto-grants-2006_08