تفاعل #1161629
ord-6dd39eacc36144babc54687108e4218a
معادلة التفاعل
المتفاعلات
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1workup.ADDITIONto the resulting solution was added, in portions over 45 minutes
- 2استخلاصThe aqueous mixture was extracted 5 times with diethyl ether
- 3غسيلthe combined organic extracts were washed 7 times with 0.2 N hydrochloric acid
- 4تجفيفtwice with water and once with saturated aqueous sodium chloride solution and dried over magnesium sulfate
- 5أخرىThe solvent was evaporated
- 6أخرىthe resulting crude residue was purified by chromatography on silica gel
- 7غسيلeluting with 1:1 ethyl acetate/hexane
- 8أخرىThe purified light-yellow oil obtained
- 9أخرىto crystallize
- 10أخرىThe solid which formed
- 11أخرىwas separated by filtration
- 12أخرىdried
الإجراء التجريبي
To 450 ml of dimethylformamide containing 23.8 ml of triethylamine was added 11.4 g of 2-(4-aminophenyl)-butanol and to the resulting solution was added, in portions over 45 minutes, 21 g of methyl(1,3-dithiolan-2-ylidene)sulfonium iodide. The resulting hazy-yellow solution was stirred for 2 hours and then poured into ice water. The aqueous mixture was extracted 5 times with diethyl ether and the combined organic extracts were washed 7 times with 0.2 N hydrochloric acid, twice with water and once with saturated aqueous sodium chloride solution and dried over magnesium sulfate. The solvent was evaporated and the resulting crude residue was purified by chromatography on silica gel, eluting with 1:1 ethyl acetate/hexane. The purified light-yellow oil obtained was immediately dissolved in warm diethyl ether and allowed to crystallize. The solid which formed was separated by filtration and dried to give 2-[4-(1,3-dithiolan-2-ylideneamino)phenyl]butanol as white spars melting at about 98.5°-100.5° C. This compound has the following structural formula ##STR3##