반응 #1089

ord-b667ae6e1894401594ee757404717db3

반응 방정식

Cl
hydrochloric acid
CC(C)OB(OC(C)C)OC(C)C
triisopropyl borate
COc1ccc2ccsc2c1
6-methoxybenzo[b]thiophene
[Li][CH2]CCC
n-butyllithium
COc1ccc2cc(B(O)O)sc2c1
6-methoxybenzo[b]thiophene-2-boronic acid
수율 71.0%

반응 조건

온도
0°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The layers were separated
  2. 2
    건조the organic layer was dried over sodium sulfate
  3. 3
    농축Concentration in vacuo
  4. 4
    기타produced a white solid
  5. 5
    기타that was triturated from ethyl ether hexanes
  6. 6
    여과Filtration

실험 절차

To a solution of 6-methoxybenzo[b]thiophene (18.13 g, 0.111 mol) in 150 mL of anhydrous tetrahydrofuran (THF) at -60° C. was added n-butyllithium (76.2 mL, 0.122 mol, 1.6M solution in hexanes), dropwise via syringe. After stirring for 30 minutes, triisopropyl borate (28.2 mL, 0.122 mol) was introduced via syringe. The resulting mixture was allowed to gradually warm to 0° C. and then distributed between 1N hydrochloric acid and ethyl acetate (300 mL each). The layers were separated, and the organic layer was dried over sodium sulfate. Concentration in vacuo produced a white solid that was triturated from ethyl ether hexanes. Filtration provided 16.4 g (71%) of 6-methoxybenzo[b]thiophene-2-boronic acid as a white solid. mp 200° C. (dec). 1H NMR (DMSO-d6) d 7.83 (s, 1H), 7.78 (d, J=8.6 Hz, 1H), 7.51 (d, J=2.0 Hz, 1H), 6.97 (dd, J=8.6, 2.0 Hz, 1H), 3.82 (s, 3H). FD mass spec: 208.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05723474uspto-grants-1998_03