تفاعل #595368

ord-87b630a1297a4008b395f5283a6f8a72

معادلة التفاعل

COC(=O)c1ccc(OCc2ccccc2)cc1OS(=O)(=O)C(F)(F)F
Methyl 4-(benzyloxy)-2-(trifluoromethylsulfonyloxy)benzoate
C=C(C)B1OC(C)(C)C(C)(C)O1
4,4,5,5-tetramethyl-2-(prop-1-en-2-yl)-1,3,2-dioxaborolane
COc1cccc(OC)c1-c1ccccc1P(C1CCCCC1)C1CCCCC1
S-Phos
O=P([O-])([O-])[O-].[K+].[K+].[K+]
K3PO4
C=C(C)c1cc(OCc2ccccc2)ccc1C(=O)OC
title compound
C=C(C)c1cc(OCc2ccccc2)ccc1C(=O)OC
methyl 4-(benzyloxy)-2-(prop-1-en-2-yl)benzoate

المذيبات

ظروف التفاعل

درجة الحرارة
75°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    استخلاصextracted with EtOAc
  2. 2
    أخرىThe combined organics were dried
  3. 3
    تركيزconcentrated
  4. 4
    أخرىThe residue was purified by flash chromatography (PE/EA=10:1)

الإجراء التجريبي

Methyl 4-(benzyloxy)-2-(trifluoromethylsulfonyloxy)benzoate (i-1c) (6.8 g, 17.4 mmol), 4,4,5,5-tetramethyl-2-(prop-1-en-2-yl)-1,3,2-dioxaborolane (2.9 g, 17.4 mmol), Pd(OAc)2 (195 mg, 0.87 mmol), S-Phos (71 mg, 0.174 mmol) and K3PO4 (11 g, 52 mmol) were mixed in THF (70 ml). The mixture was stirred at 75° C. for 24 h. The mixture was diluted with H2O, and extracted with EtOAc. The combined organics were dried and concentrated. The residue was purified by flash chromatography (PE/EA=10:1) to afford the title compound. LCMS (ESI) calc'd for C18H18O3 [M+H]+: 391. found: 391.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09095583B2uspto-grants-2015_08