Реакция #74683

ord-8cabb55f57a94b10a776acc8ba283193

Уравнение реакции

CCN(CC)CC
triethylamine
CC(=O)[O-].[K+]
potassium acetate
OB(O)c1ccoc1
3-furylboronic acid
Oc1ccc(C(F)(F)F)cc1I
2-Iodo-4-(trifluoromethyl)phenol
CC(=O)OC(C)=O
acetic anhydride
CC(=O)Oc1ccc(C(F)(F)F)cc1-c1ccoc1
title product
Выход 86.6%
CC(=O)Oc1ccc(C(F)(F)F)cc1-c1ccoc1
2-(3-Furyl)-4-(trifluoromethyl)phenyl acetate
Выход 86.6%

Условия реакции

Температура
90°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.ADDITIONwas added
  2. 2
    Другоеthe reaction degassed 3 more times
  3. 3
    ТемператураThe reaction was then cooled
  4. 4
    Другоеpartitioned between EtOAc (50 mL) and water (50 mL)
  5. 5
    Другоеthe organic layer was separated
  6. 6
    Другоеdried in vacuo
  7. 7
    Другоеto give a brown oil
  8. 8
    ДругоеThe reaction was then partitioned between EtOAc (30 ml) and water (30 ml)
  9. 9
    Другоеorganic layer was dried in vacuo
  10. 10
    Другоеto give a brown oil which
  11. 11
    Другоеcrystallised
  12. 12
    ДругоеThis was triturated with heptane

Методика

2-Iodo-4-(trifluoromethyl)phenol (9.9 g, 0.0344 mol) was dissolved in 2-methyl tetrahydrofuran (100 mL) then potassium acetate (11.8 g, 0.12 mol) and 3-furylboronic acid (5.0 g, 0.0447 mol) was added and the reaction degasses 3 times before bis(tri-tert-butylphosphine) palladium (0) (1.0 g, 0.00196 mol) was added and the reaction degassed 3 more times. The reaction was then stirred at 90° C. under nitrogen for 18 hours. The reaction was then cooled and partitioned between EtOAc (50 mL) and water (50 mL), the organic layer was separated and dried in vacuo to give a brown oil. This was dissolved in tert-butyl methyl ether (50 mL), triethylamine (7.2 mL, 0.051 mol) added then acetic anhydride (4.7 mL, 0.051 mol) and stirred for 2 hours at room temperature. The reaction was then partitioned between EtOAc (30 ml) and water (30 ml) then organic layer was dried in vacuo to give a brown oil which crystallised upon standing. This was triturated with heptane to give the title product as a pale brown solid (8.04 g, 86.6%). LCMS Rt=1.70 min. 1H NMR (400 MHz, CDCl3): δ 2.34 (s, 3H), 6.67 (s, 1H) 7.26 (m, 1H) 7.51 (s, 1H), 7.57 (d, 1H), 7.76 (m 2H)

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08541588B2uspto-grants-2013_09