反応 #2446133

ord-ec5409d66481487da9ba95ba39185a04

反応方程式

CCOCC
ether
O=C1CCc2ccccc2N1
3,4-dihydro-1H-quinolin-2-one
O=C1CCC(=O)N1Br
N-bromosuccinimide
O
water
O=C1CCc2cc(Br)ccc2N1
6-Bromo-3,4-dihydro-1H-quinolin-2-one

溶媒

反応条件

温度
0°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    抽出the solution was extracted with ethyl acetate (3×150 ml)
  2. 2
    洗浄The organic phase was washed with water (2×200 ml)
  3. 3
    乾燥dried over MgSO4
  4. 4
    その他evaporated
  5. 5
    その他affording a yellow solid which
  6. 6
    その他was purified

実験手順

To a solution of 3,4-dihydro-1H-quinolin-2-one (10.0 g, 67.9 mmol) in 100 ml dry DMF was added dropwise a solution of N-bromosuccinimide (12.7 g, 71.3 mmol) in 150 ml dry DMF at 0° C. The mixture was stirred at 0° C. for 2 h, then 400 ml water was added and the solution was extracted with ethyl acetate (3×150 ml). The organic phase was washed with water (2×200 ml), then dried over MgSO4 and evaporated, affording a yellow solid which was purified by washing with cold ether providing pure 6-bromo-3,4-dihydro-1H-quinolin-2-one (13.6 g, 60.3 mmol, 89%) as colorless needles.

出典

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