تفاعل #1596948

ord-2b094232b48642f2a451f1a7b0685be9

معادلة التفاعل

CCC1COC(c2ccc(B3OC(C)(C)C(C)(C)O3)c(F)c2)CC1Br
4-bromo-5-ethyl-2-[3-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]tetrahydropyran
[H][H]
hydrogen
CCN(CC)CC
triethylamine
CCC1CCC(c2ccc(B3OC(C)(C)C(C)(C)O3)c(F)c2)OC1
5-ethyl-2-[3-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]tetrahydropyran

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe organic phase is separated off
  2. 2
    ترشيحfiltered absorptively (SiO2, toluene)
  3. 3
    تركيزThe filtrate is concentrated to dryness
  4. 4
    أخرىthe residue is recrystallised from ethanol at reduced temperature

الإجراء التجريبي

18.0 g (36.2 mmol) of 4-bromo-5-ethyl-2-[3-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]tetrahydropyran are hydrogenated for 30 h at a hydrogen pressure of 5 bar and at 80° C. in toluene/water in the presence of Pd/C (5% of Pd) and 12.7 ml (88.1 mmol) of triethylamine. The organic phase is separated off and filtered absorptively (SiO2, toluene). The filtrate is concentrated to dryness, and the residue is recrystallised from ethanol at reduced temperature, giving 5-ethyl-2-[3-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]tetrahydropyran as a colourless solid.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08211513B2uspto-grants-2012_07