تفاعل #216804

معادلة التفاعل

sodium iodide

chloromethyl ethyl ether

potassium tert-butoxide

2,3-dibromo-5-(p-chlorophenyl)-4-[(trifluoromethyl)sulfonyl]pyrrole

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title product

المردود 74.2%

2,3-Dibromo-5-(p-chlorophenyl)-1-(ethoxymethyl)-4-[(trifluoromethyl)sulfonyl]pyrrole

المردود 74.2%

المذيبات

hexane

water

tetrahydrofuran

tetrahydrofuran

ظروف التفاعل

المعالجة

1. 1
   workup.STIRRINGstirred for five minutes
2. 2
   workup.STIRRINGstirred at room temperature for several hours
3. 3
   استخلاصextracted with ether
4. 4
   غسيلThe combined organic extracts are washed with water and brine
5. 5
   تجفيفdried over anhydrous sodium sulfate
6. 6
   تركيزconcentrated in vacuo
7. 7
   أخرىto give an orange oil
8. 8
   ترشيحfiltered

الإجراء التجريبي

A solution of potassium tert-butoxide (0.62 g, 0.0055 mol) in tetrahydrofuran is treated with 2,3-dibromo-5-(p-chlorophenyl)-4-[(trifluoromethyl)sulfonyl]pyrrole (2.34 g, 0.005 mol), stirred for 15 minutes, treated with sodium iodide (0.82 g, 0.0055 mol), stirred for five minutes, treated with a solution of chloromethyl ethyl ether (0.52 g, 0.0055 mol) in tetrahydrofuran, stirred at room temperature for several hours, poured into water and extracted with ether. The combined organic extracts are washed with water and brine, dried over anhydrous sodium sulfate and concentrated in vacuo to give an orange oil. The oil is slurried in hexane and filtered to obtain the title product as a pale yellow solid (1.95 g, mp 133°-135° C.) which is identified by 1HNMR and 19FNMR spectral analyses.

المصدر