تفاعل #218552

ord-80b4adacaad34e8898a241a418330c09

معادلة التفاعل

Brc1csc2ccccc12
3-bromo benzo[b]thiophene
O=[N+]([O-])O
nitric acid
CCOC(C)=O
ice water
CCOC(C)=O
ethyl acetate
O=[N+]([O-])c1sc2ccccc2c1Br
3-Bromo-2-nitro-benzo[b]thiophene

الكواشف

لا شيء

ظروف التفاعل

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

المعالجة

  1. 1
    workup.ADDITIONThen pour
  2. 2
    استخلاصExtract with dichloromethane (3×500 mL)
  3. 3
    تجفيفthe organic layer dry over MgSO4
  4. 4
    أخرىEvaporation
  5. 5
    أخرىgive a yellow solid
  6. 6
    أخرىThe resulting yellow solid triturate with diethyl ether
  7. 7
    أخرىto give a yellow solid

الإجراء التجريبي

Add dropwise fuming nitric acid (90%, 8.6 mL, 183 mmol) to a mixture of 3-bromo benzo[b]thiophene (39 g, 183 mmol) in TFA (100 mL) and dichloromethane (400 mL) at 0° C. The reaction turn greenish, then yellow precipitates. To this reaction mixture, add dichloromethane (200 mL) and the reaction stir at 0° C. for 30 min. Then pour the reaction into ice-water (2L). Extract with dichloromethane (3×500 mL) and the organic layer dry over MgSO4. Evaporation give a yellow solid. The resulting yellow solid triturate with diethyl ether to give a yellow solid. (Total: 34.8 g, 73%). Mass spectrum (m/e): 259(M+1); 1HNMR(300 MHz, DMSO-d6) δ ppm: 7.70(tt, 2H), 8.04(d, 1H), 8.17(d, 1H). 13CNMR(75 MHz, DMSO-d6) δ ppm: 112.5, 124.8, 126.9, 127.9, 131.3, 137.0, 137.2, 166.1.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07384934B2uspto-grants-2008_06