반응 #3160

ord-bcf47efb084b407da3df0c21bd581e1b

반응 방정식

O
water
CC(C)OB(OC(C)C)OC(C)C
triisopropylborate
CCCCCCC(Br)CC1Cc2ccccc2O1
b-bromo-2-octylcoumaran
[Li][CH2]CCC
butyllithium
CCCCCCCCC1Cc2cc(B(O)O)ccc2O1
2-octylcoumaran-5-boronic acid
수율 67.1%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타nitrogen atmosphere on a dry ice-acetone bath at an inner temperature of -70° to -68° C., followed
  2. 2
    workup.STIRRINGby stirring for 50 minutes at the same temperature
  3. 3
    workup.STIRRINGby stirring for minutes at the same temperature
  4. 4
    기타Thereafter, the cooling bath was removed
  5. 5
    workup.ADDITIONfollowed by gradual addition of 9.5 ml of 10%-hydrochloric acid
  6. 6
    기타After the reaction
  7. 7
    추출subjected to extraction with isopropyl ether
  8. 8
    세척by washing with water
  9. 9
    건조drying with mirabilite and distilling-off of the solvent
  10. 10
    기타to obtain a residue
  11. 11
    workup.WAITthe mixture was left
  12. 12
    기타to precipitate a crystal
  13. 13
    여과The crystal was recovered by filtration

실험 절차

Then, 2.00 g (6.43 mM) of b-bromo-2-octylcoumaran and 28 ml of dry THF were placed in a 100 ml-three-necked flask. To the mixture, 4.5 ml (7.20 mM) of a 1.6M solution of butyllithium in hexane was added dropwise under stirring and nitrogen atmosphere on a dry ice-acetone bath at an inner temperature of -70° to -68° C., followed by stirring for 50 minutes at the same temperature. To the resultant mixture a solution of 3.2 ml (13.9 mM) of triisopropylborate in 5.7 ml of dry THF was added dropwise in 10 minutes at an inner temperature of -73° to -68° C., followed by stirring for minutes at the same temperature. Thereafter, the cooling bath was removed and the inner temperature was increased to room temperature, followed by gradual addition of 9.5 ml of 10%-hydrochloric acid. After the reaction, the reaction mixture was poured into water and subjected to extraction with isopropyl ether, followed by washing with water, drying with mirabilite and distilling-off of the solvent to obtain a residue. To the residue, hexane was added and the mixture was left standing in a freezer to precipitate a crystal. The crystal was recovered by filtration to obtain 1.19 g of 2-octylcoumaran-5-boronic acid (Yield: 67.1%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05733476uspto-grants-1998_03