反応 #2446134

ord-07a10a81436f41939437260f955e2692

反応方程式

CI
methyl iodide
O=C1CCc2cc(Br)ccc2N1
6-bromo-3,4-dihydro-1H-quinolin-2-one
CC(C)(C)[O-].[K+]
potassium tert-butylate
CN1C(=O)CCc2cc(Br)ccc21
6-bromo-1-methyl-3,4-dihydro-1H-quinolin-2-one
収率 78.0%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.WAITFollowing overnight
  2. 2
    workup.STIRRINGstirring
  3. 3
    抽出Extraction with ethyl acetate (2×100 mL)
  4. 4
    洗浄by washing of the organic extracts with water and brine
  5. 5
    乾燥drying over MgSO4 and removal of the solvent in vacuo
  6. 6
    その他gave a light yellow solid
  7. 7
    その他Purification by flash chromatography (hexanes/ethyl acetate, 7/3, Rf=0.21)

実験手順

To a solution of 6-bromo-3,4-dihydro-1H-quinolin-2-one (339 mg, 1.50 mmol) in 15 ml dry DMF was added potassium tert-butylate (336 mg, 3.0 mmol). After the mixture was stirred for 30 min at room temperature, a solution of methyl iodide (426 mg, 3.0 mmol) in 5 ml dry DMF was added. Following overnight stirring, the mixture was diluted with 100 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, 7/3, Rf=0.21) gave 6-bromo-1-methyl-3,4-dihydro-1H-quinolin-2-one (281 mg, 1.17 mmol, 78%) as colorless needles.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08685960B2uspto-grants-2014_04