تفاعل #1089

ord-b667ae6e1894401594ee757404717db3

معادلة التفاعل

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
المردود 71.0%

ظروف التفاعل

درجة الحرارة
0°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe layers were separated
  2. 2
    تجفيفthe organic layer was dried over sodium sulfate
  3. 3
    تركيزConcentration in vacuo
  4. 4
    أخرىproduced a white solid
  5. 5
    أخرىthat was triturated from ethyl ether hexanes
  6. 6
    ترشيحFiltration

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05723474uspto-grants-1998_03