تفاعل #2446136

ord-993a07960f2c40e38adf062da94e12e6

معادلة التفاعل

CC(C)Br
isopropyl bromide
O=C1CCc2cc(Br)ccc2N1
6-bromo-3,4-dihydro-1H-quinolin-2-one
CC(C)(C)[O-].[K+]
potassium tert-butylate
CC(C)N1C(=O)CCc2cc(Br)ccc21
6-bromo-1-isopropyl-3,4-dihydro-1H-quinolin-2-one
المردود 38.9%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةthe mixture heated to 80° C
  2. 2
    workup.STIRRINGAfter stirring for additional 48 h
  3. 3
    درجة الحرارةthe mixture was cooled to room temperature
  4. 4
    استخلاصExtraction with ethyl acetate (2×100 mL)
  5. 5
    غسيلby washing of the organic extracts with water and brine
  6. 6
    تجفيفdrying over MgSO4 and removal of the solvent in vacuo
  7. 7
    أخرىgave a light yellow solid
  8. 8
    أخرىPurification by flash chromatography (hexanes/ethyl acetate, 4/1, Rf=0.21)

الإجراء التجريبي

To a solution of 6-bromo-3,4-dihydro-1H-quinolin-2-one (750 mg, 3.32 mmol) in 20 ml dry DMF was added potassium tert-butylate (804 mg, 6.64 mmol). After the mixture was stirred for 30 min at room temperature, a solution of isopropyl bromide (814 mg, 6.64 mmol) in 10 ml dry DMF was added and the mixture heated to 80° C. After stirring for additional 48 h, the mixture was cooled to room temperature and diluted with 150 ml 1 N HCl. Extraction with ethyl acetate (2×100 mL) followed by washing of the organic extracts with water and brine, drying over MgSO4 and removal of the solvent in vacuo gave a light yellow solid. Purification by flash chromatography (hexanes/ethyl acetate, 4/1, Rf=0.21) gave 6-bromo-1-isopropyl-3,4-dihydro-1H-quinolin-2-one (347 mg, 1.29 mmol, 33%) as pale yellow solid.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08685960B2uspto-grants-2014_04