반응 #2348085

ord-9e78c93bde7f467e939d2519372aec94

반응 방정식

COB(OC)OC
trimethyl borate
Cl
hydrochloric acid
C1CCOC1
THF
[Li][CH](C)CC
sec-butyl lithium
OB(O)c1ccccc1
phenylboronic acid

반응 조건

온도
-71°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.WAITthe stirring was continued for additional 180 minutes
  2. 2
    기타The resulting reaction mixture
  3. 3
    기타to come to 0° C.
  4. 4
    workup.ADDITIONpoured into a vessel
  5. 5
    온도had been chilled at 0° C.
  6. 6
    workup.ADDITIONmixed
  7. 7
    기타to be separated into an organic layer
  8. 8
    추출Extraction
  9. 9
    세척The extracts were washed with brine
  10. 10
    건조dried over anhydrous magnesium sulfate
  11. 11
    workup.DISTILLATIONThen, the solvent was distilled off under reduced pressure

실험 절차

The compound (T17) and THF (1,000 ml) were put into a reaction vessel under an atmosphere of nitrogen, and chilled to −71° C. Then, a sec-butyl lithium solution (1.0 M in cyclohexane and n-hexane; 1,000 ml) were added dropwise thereto in the temperature range of −71° C. to −62° C., and the stirring was continued for additional 120 minutes. Subsequently, trimethyl borate (127.6 g) was added dropwise in the temperature range of −70° C. to −59° C., and the stirring was continued for additional 180 minutes. The resulting reaction mixture was allowed to come to 0° C., and then poured into a vessel containing 1N-hydrochloric acid (3,000 ml) and ethyl acetate (3,000 ml) which had been chilled at 0° C. and mixed. The mixture was then allowed to stand to be separated into an organic layer and an aqueous layer. Extraction was carried out and the resulting organic layer was fractionated. The extracts were washed with brine, and dried over anhydrous magnesium sulfate. Then, the solvent was distilled off under reduced pressure, whereby 115.9 g of phenylboronic acid derivative (T18) was obtained.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07846514B2uspto-grants-2010_12