تفاعل #74683

معادلة التفاعل

triethylamine

potassium acetate

3-furylboronic acid

2-Iodo-4-(trifluoromethyl)phenol

acetic anhydride

→

title product

المردود 86.6%

2-(3-Furyl)-4-(trifluoromethyl)phenyl acetate

المردود 86.6%

المذيبات

tert-butyl methyl ether

2-methyl tetrahydrofuran

ظروف التفاعل

المعالجة

1. 1
   workup.ADDITIONwas added
2. 2
   أخرىthe reaction degassed 3 more times
3. 3
   درجة الحرارةThe reaction was then cooled
4. 4
   أخرىpartitioned between EtOAc (50 mL) and water (50 mL)
5. 5
   أخرىthe organic layer was separated
6. 6
   أخرىdried in vacuo
7. 7
   أخرىto give a brown oil
8. 8
   أخرىThe reaction was then partitioned between EtOAc (30 ml) and water (30 ml)
9. 9
   أخرىorganic layer was dried in vacuo
10. 10
    أخرىto give a brown oil which
11. 11
    أخرىcrystallised
12. 12
    أخرىThis was triturated with heptane

الإجراء التجريبي

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)

المصدر