تفاعل #1256714

ord-2824de49fee24888a1ed9978987ea640

معادلة التفاعل

Cc1cncc(C)c1-c1c(C)cc(I)cc1C
11
Cc1cncc(C)c1-c1c(C)cc(I)cc1C
4-(4-iodo-2,6-dimethyl-phenyl)-3,5-dimethyl-pyridine
C=Cc1cc(C(C)(C)C)c(O)c(C(C)(C)C)c1
12
C=Cc1cc(C(C)(C)C)c(O)c(C(C)(C)C)c1
2,6-di-tert-butyl-4-vinyl-phenol
c1ccc(P(c2ccccc2)c2ccccc2)cc1
PPh3
Cc1cncc(C)c1-c1c(C)cc(C=Cc2cc(C(C)(C)C)c(O)c(C(C)(C)C)c2)cc1C
title compound
المردود 91.2%
Cc1cncc(C)c1-c1c(C)cc(C=Cc2cc(C(C)(C)C)c(O)c(C(C)(C)C)c2)cc1C
2,6-di-tert-butyl-4-{2-[4-(3,5-dimethyl-pyridin-4-yl)-3,5-dimethyl-phenyl]-vinyl}-phenol
المردود 91.2%

ظروف التفاعل

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

المعالجة

  1. 1
    أخرىevacuated
  2. 2
    workup.ADDITIONNext, dry Et3N (10 mL) was added under an N2 flow
  3. 3
    أخرىthe mixture was degassed by 3 freeze-thaw cycles
  4. 4
    درجة الحرارةThe reaction mixture was then cooled to room temperature
  5. 5
    workup.ADDITIONdiluted with methylene chloride (50 mL)
  6. 6
    ترشيحfiltered through a thin pad of silica gel
  7. 7
    تركيزconcentrated in vacuo
  8. 8
    أخرىto afford a red solid
  9. 9
    أخرىThe crude product was purified by flash chromatography on silica gel
  10. 10
    غسيلeluting with 3:1 hexane

الإجراء التجريبي

A flame-dried sealable Schlenk tube was charged with 11 (1.69 g, 5.0 mmol), 12 (2.32 g, 10.0 mmol), Pd(OAc)2 (112 mg, 0.50 mmol), and PPh3 (131 mg, 0.50 mmol), evacuated, and then backfilled with N2. Next, dry Et3N (10 mL) was added under an N2 flow. The Schlenk tube was next sealed, the mixture was degassed by 3 freeze-thaw cycles, and backfilled with N2. The Schlenk tube was then wrapped with aluminum foil and stirred at 100° C. for 36 h. The reaction mixture was then cooled to room temperature, diluted with methylene chloride (50 mL), filtered through a thin pad of silica gel, and concentrated in vacuo to afford a red solid. The crude product was purified by flash chromatography on silica gel, eluting with 3:1 hexane: ethyl acetate to give the title compound 2.01 g (91.2%) as a colorless solid: mp 234-235° C.; 1H NMR (400 MHz, CDCl3): δ 8.402 (s, 2H), 7.371 (s, 2H), 7.307 (s, 2H), 7.133 (d, 1H, J=16.4 Hz), 6.936 (d, 1H, J=16.0 Hz), 5.331 (s, 1H), 1.951 (s, 6H), 1.911 (s, 6H), 1.499 (s, 18H); 13C NMR (100 MHz, CDCl3): δ 153.971, 148.630, 148.502, 137.347, 136.301, 135.928, 134.817, 131.251, 129.595, 128.876, 125.837, 125.709, 123.598, 34.638, 30.534, 19.997, 16.822; HRMS (EI): m/z 441.3023 [M+]; calcd, 441.3032; Anal. Calcd. for C31H39NO·H2O: C, 81.00; H, 8.99; N, 3.05. Found; C, 81.01; H, 8.64; N, 3.02.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07824582B2uspto-grants-2010_11