반응 #9198

ord-5037c9c33a5a49e9b0b5c20797e25f9c

반응 방정식

N#Cc1ccccc1
benzonitrile
N#C[S-].[K+]
potassium thiocyanate
N#Cc1ccc(N)cc1
4-aminobenzonitrile
BrBr
bromine
N#Cc1ccc2nc(N)sc2c1
title compound
수율 67.4%
N#Cc1ccc2nc(N)sc2c1
2-Amino-1,3-benzothiazole-6-carbonitrile
수율 67.4%

반응 조건

온도
16°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타the flask was equipped with an addition funnel
  2. 2
    여과filtered
  3. 3
    세척The presscake was washed well with water
  4. 4
    여과filtered
  5. 5
    세척Again the presscake was washed well with water
  6. 6
    기타After drying in vacuo

실험 절차

Two grams of 4-aminobenzonitrile was dissolved in about 40 mL acetic acid and the solution was cooled to about 16° C. About 3.3 g of potassium thiocyanate was added and the flask was equipped with an addition funnel. The addition funnel was charged with about 2.7 g bromine and about 5 mL acetic acid. This dark solution was then added to the benzonitrile solution in a dropwise fashion under good agitation and allowed to stir for about 16 hours. The slurry was then drowned into water and filtered. The presscake was washed well with water, reslurried in dilute aqueous alkali and filtered. Again the presscake was washed well with water. After drying in vacuo, about 2 grams of the title compound was isolated. 1H NMR 6.8 (d, 1H, J=8.7 Hz), 6.9 (br s, 2H), 7.6 (dd, 1H, J=2 Hz, J=8.7 Hz), 8.0 (d, 1H, J=2 Hz), LC/MS 2.34 min, 174 (M−H−), RP-HPLC RT 7.7 minutes.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07091227B2uspto-grants-2006_08