تفاعل #1535

ord-5c044a04ef604d88b3d7ec14794c7e4f

معادلة التفاعل

[Cl-].[NH4+]
ammonium chloride
CC(C)(C)NS(=O)(=O)c1sccc1Br
N-t-butyl-3-bromo-2-thiophenesulfonamide
[Li][CH2]CCC
n-butyl lithium
CCOC(C)=O
ethyl acetate
CC(C)(C)NS(=O)(=O)c1sccc1C(=O)CCl
pure title compound
المردود 69.0%
CC(C)(C)NS(=O)(=O)c1sccc1C(=O)CCl
N-t-butyl-3-chloroacetyl-2-thiophenesulfonamide
المردود 69.0%

ظروف التفاعل

درجة الحرارة
-78°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةthe temperature of the mixture was raised slowly to -20° C.
  2. 2
    درجة الحرارةagain cooled to -78° C
  3. 3
    درجة الحرارةThe temperature of the reaction mixture was raised slowly to -20° C. again
  4. 4
    أخرىto separate the organic layer
  5. 5
    تجفيفThe extracted organic layer was dried over anhydrous magnesium sulfate
  6. 6
    تركيزconcentrated

الإجراء التجريبي

2.98 g (0.0| mole) of N-t-butyl-3-bromo-2-thiophenesulfonamide was dissolved in 50 ml of dry tetrahydrofura mixture was cooled to -78° C. under nitrogen gas. To the reaction solution was slowly added dropwise 8.4 ml of n-butyl lithium(2.5N) and then the temperature of the mixture was raised slowly to -20° C. and again cooled to -78° C. 1.4 g (0.012 mole) of ethyl chloroacetates was added slowly to the mixture. The temperature of the reaction mixture was raised slowly to -20° C. again and then the mixture was stirred for 10 minutes. To the mixture was added 100 ml of aqueous ammonium chloride solution and then added 100 ml of ethyl acetate to separate the organic layer. The extracted organic layer was dried over anhydrous magnesium sulfate and then concentrated. The residue was subjected to column chromatography on silica gel to obtain 1.9 g (Yield: 69%) of the pure title compound as a liquid.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05726127uspto-grants-1998_03