تفاعل #77771

ord-191c59b28e964af6a3cd91ce94ab1f94

المذيبات

ظروف التفاعل

درجة الحرارة
50°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةcooled to RT
  2. 2
    استخلاصThe aqueous phase was extracted with ether
  3. 3
    غسيلthe organic phases were washed with water
  4. 4
    تجفيفdried over Na2SO4

الإجراء التجريبي

514 mg (2.3 mmol) 5-Hydroxy-2,3-dihydro-indole-1-carboxylic acid tert-butyl ester in 12 ml DMF were treated with 830 mg (6 mmol) powdered K2CO3 and 1070 mg (5 mmol) 1,4-dibromobutene. The suspension was stirred at 50° C. for 3 h, cooled to RT, diluted with ether and water. The aqueous phase was extracted with ether, the organic phases were washed with water and dried over Na2SO4. Column chromatography on silica gel with hexane/EtOAc 9:1 yielded 270 mg (31%) 5-(4-Bromo-but-2-enyloxy)-2,3-dihydro-indole-1-carboxylic acid tert-butyl ester as colorless solid, MS: 368 (MH+, 1Br).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06706751B2uspto-grants-2004_03