تفاعل #166274

ord-ae47c4adfc9d403c835af054aab39927

معادلة التفاعل

CC(C)(C)c1ccc(C(=O)O)c(Br)c1
4-tert-butyl-2-bromobenzoic acid
Oc1ccc(F)cc1
4-fluoro phenol
O=C([O-])[O-].[Cs+].[Cs+]
cesium carbonate
O=C(O)c1cccc2ccccc12
1-naphthoic acid
CC(C)(C)c1ccc(C(=O)O)c(Oc2ccc(F)cc2)c1
2-(4-fluorophenoxy)-4-tert-butylbenzoic acid
المردود 39.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    تركيزThe reaction was concentrated under reduced pressure
  2. 2
    أخرىpurified by silica gel chromatography (0%-5% MeOH—CH2Cl2)

الإجراء التجريبي

A stirred suspension of 4-tert-butyl-2-bromobenzoic acid (0.26 g, 1.0 mmol), 4-fluoro phenol (0.22 g, 2.0 mmol), cesium carbonate (0.65 g, 2.0 mmol), copper trifluoromethanesulfonate-benzene complex (13 mg, 25 μmol), 1-naphthoic acid (0.34 g, 2.0 mmol), and 4 Å molecular sieves (0.25 g) in toluene (10 mL) and EtOAc (5 μL) was heated at 110° C. for 16 h. The reaction was concentrated under reduced pressure and purified by silica gel chromatography (0%-5% MeOH—CH2Cl2) to afford 2-(4-fluorophenoxy)-4-tert-butylbenzoic acid (0.11 g, 39% yield) as a white solid. LC/MS: m/z 289.0 (M+H)+ at 3.58 min (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)). 1H NMR (400 MHz, CDCl3) δ 8.12 (d, J=8.3 Hz, 1H), 7.24 (d, J=1.7 Hz, 1H), 7.14-7.05 (m, 4H), 6.84 (d, J=1.6 Hz, 1H), 1.23 (s, 9H) ppm.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08841483B2uspto-grants-2014_09