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N-Methoxy-N-methylpropionamide → HCID 22473751、化合物

HRID 2183636
ノート
印刷プレビュー

反応式

HRID 2183636 の反応式
Br[C:2]1[C:3]2[C:10]([CH3:11])=[CH:9][CH:8]=[CH:7][C:4]=2[S:5][CH:6]=1.C([Li])CCC.CON(C)[C:20](=[O:23])[CH2:21][CH3:22]>O1CCCC1.CCOCC>[CH3:11][C:10]1[C:3]2[CH:2]=[C:6]([C:20](=[O:23])[CH2:21][CH3:22])[S:5][C:4]=2[CH:7]=[CH:8][CH:9]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 11344007N-Methoxy-N-methylpropionamideHCID 22473703HCID 22473703、化合物HCID 178418339Butyllithium

生成物 1

HCID 22473751HCID 22473751、化合物収率 34.9%

試薬・触媒・溶媒 2

HCID 3283Diethyl Ether溶媒HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
-70 °C

実験手順

A solution of 3-bromo-4-methylbenzo[b]thiophene (1.69 g) in tetrahydrofuran (10 ml) was added dropwise under nitrogen at −70° C. over 10 minutes to a stirred solution of n-butyllithium (2.5M solution in hexanes; 3.87 ml) in ether (30 ml), then the mixture was stirred at −70° C. for 30 minutes. A solution of N-methoxy-N-methylpropionamide (1.31 g) in tetrahydrofuran (10 ml) was added dropwise at −70° C. over 10 minutes, the mixture was stirred at −70° C. for 3 hours, then it was allowed to warm to ambient temperature and quenched by the addition of saturated aqueous ammonium chloride solution (30 ml). The organic layer was separated, washed with saturated aqueous sodium chloride solution (30 ml), and dried (MgSO4). The solvents were removed in vacuao to give 1-(4-methylbenzo[b]thiophen-2-yl)propan-1-one (0.53 g) as an orange solid which was used without further purification.

後処理

  1. stirringthe mixture was stirred at −70° C. for 3 hours
  2. temperatureto warm to ambient temperature
  3. customquenched by the addition of saturated aqueous ammonium chloride solution (30 ml)
  4. customThe organic layer was separated
  5. washwashed with saturated aqueous sodium chloride solution (30 ml)
  6. dry with materialdried (MgSO4)
  7. customThe solvents were removed in vacuao

出典と根拠

ORDレコード
ord-aa8be48533d54085a1117758a789f9cb
出典データセット
uspto-grants-2005_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06900216B2

反応ノート

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