تفاعل #166064

ord-e2dcfa49427c468ab0bc95107cd43e26

معادلة التفاعل

Cl
HCl
Fc1cc(Br)cc(OCc2ccccc2)c1
5-benzyloxy-3-fluorophenyl Bromide
C=Cc1ccc(F)cc1
4-fluorostyrene
CCN(CC)CC
Et3N
Fc1ccc(C=Cc2cc(F)cc(OCc3ccccc3)c2)cc1
desired product
المردود 91.0%
Fc1ccc(C=Cc2cc(F)cc(OCc3ccccc3)c2)cc1
5-benzyloxy-3,4′-difluorostilbene
المردود 91.0%

المذيبات

ظروف التفاعل

درجة الحرارة
100°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe organic layer was separated
  2. 2
    غسيلwashed with water and brine
  3. 3
    تجفيفdried over Na2SO4
  4. 4
    ترشيحfiltered
  5. 5
    أخرىevaporated

الإجراء التجريبي

A mixture of 5-benzyloxy-3-fluorophenyl Bromide (2.81 g, 10 mmol), Pd(OAc)2 (0.067 g, 0.3 mmol), tri-o-tolylphosphine (0.18 g, 0.6 mmol), 4-fluorostyrene (1.53 g, 12.5 mmol), and Et3N (1.26 g, 12.5 mmol) in 20 ml dry DMF was stirred at 100° C. for 24 hours under N2. The dark mixture was distributed between EtOAc and 1N HCl. The organic layer was separated and washed with water and brine, dried over Na2SO4, filtered, and evaporated. After flash column, the desired product (2.93 g, 91%) was obtained. Data are: 1H NMR (CDCl3, 300 MHz) δ 7.49-7.34 (m, 7H), 7.08-6.81 (m, 6H), 6.60 (dt, 1H), 5.08 (s, 2H); 19F NMR (CDCl3, 282 MHz) δ −31666.54 (t), −32136.54 (t). HRMS (EI+) found 322.1169 M+, calcd 322.1169 for C21H16F2O.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08841477B2uspto-grants-2014_09