تفاعل #2336530

ord-06ecc1da7dbe4a3482e6a1d02dc0a08d

معادلة التفاعل

Cc1ccc(S(=O)(=O)Cl)cc1
p-Toluenesulfonyl chloride
N#Cc1c(O)ccc(O)c1C#N
2,3-dicyanohydroquinone
O=C([O-])[O-].[K+].[K+]
potassium carbonate
Cc1ccc(S(=O)(=O)Oc2ccc(OS(=O)(=O)c3ccc(C)cc3)c(C#N)c2C#N)cc1
title compound
Cc1ccc(S(=O)(=O)Oc2ccc(OS(=O)(=O)c3ccc(C)cc3)c(C#N)c2C#N)cc1
3,6-Bis(4′-methylphenylsulfonyloxy) phthalonitrile

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe mixture was then heated
  2. 2
    درجة الحرارةto reflux
  3. 3
    غسيلTLC (eluting: CH2Cl2)
  4. 4
    أخرىhad been consumed
  5. 5
    workup.ADDITIONwas poured into water (200 mL)
  6. 6
    workup.STIRRINGthe mixture stirred for 1 hour
  7. 7
    ترشيحFiltration

الإجراء التجريبي

p-Toluenesulfonyl chloride (25.80 g, 135 mmol) was added to a suspension of 2,3-dicyanohydroquinone (10.00 g, 62.5 mmol) and potassium carbonate (34.50 g, 250 mmol) in acetone (75 mL). The temperature of the flask rose rapidly, which stabilised after 2 minutes. The mixture was then heated to reflux and stirred for 2 hours. TLC (eluting: CH2Cl2) indicated that all the starting 2,3-dicyanohydroquinone had been consumed. The mixture was allowed to cool to room temperature, and was poured into water (200 mL), and the mixture stirred for 1 hour. Filtration gave the title compound (Product A) as a colourless solid, which was washed with more water (˜30 mL) and pulled dry. The solid was then dried in an oven (28.36 g, 97%). This material was used without further purification. [Found: C, 55.8%; H, 3.3%; N, 6.0%; S, 13.5%; C22H16O6N2S2 requires C, 56.4%; H, 3.4%; N, 6.0%; S, 13.7%]; MS (EI+) 468 (M+, 80%), 155 (CH3C6H4SO2, 100%), 91 (CH3C6H4, 90%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07314511B2uspto-grants-2008_01