반응 #1596948

ord-2b094232b48642f2a451f1a7b0685be9

반응 방정식

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

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The organic phase is separated off
  2. 2
    여과filtered absorptively (SiO2, toluene)
  3. 3
    농축The filtrate is concentrated to dryness
  4. 4
    기타the residue is recrystallised from ethanol at reduced temperature

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08211513B2uspto-grants-2012_07