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1,1-Dichloroethane → 2-(1-Chloro-ethyl)-1H-benzoimidazole

HRID 253464
ノート
印刷プレビュー

反応式

HRID 253464 の反応式
[NH:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[CH:10](O)[CH3:11].[Cl:13]C(Cl)C.S(Cl)(Cl)=O>>[Cl:13][CH:10]([C:2]1[NH:3][C:4]2[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=2[N:1]=1)[CH3:11]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 63651,1-DichloroethaneHCID 24386Thionyl ChlorideHCID 2059221-(1H-1,3-benzodiazol-2-yl)ethan-1-ol

生成物 1

HCID 43472862-(1-Chloro-ethyl)-1H-benzoimidazole

実験手順

1-(1H-Benzimidazol-2-yl)-ethanol (146) (1.00 g, 6.16 mmol) was suspended in dichloro ethane (50 mL, 800 mmol). Thionyl chloride (4.00 mL, 54.8 mmol) was added dropwise and the reaction was stirred at room temperature and then heated to 60° C. for 6 hours. After cooling to room temperature the reaction was evaporated to dryness under reduced pressure. The obtained solid was washed with ethyl acetate. The powder was suspended in ethyl acetate and washed with saturated sodium bicarbonate solution and brine. The organic portion was dried over anhydrous sodium sulfate and concentrated. The obtained off-white solid was used without further purification (147, 0.864 g, 76%). MS (ESI) [M+H+]+=181.2.

後処理

  1. temperatureheated to 60° C. for 6 hours
  2. temperatureAfter cooling to room temperature the reaction
  3. customwas evaporated to dryness under reduced pressure
  4. washThe obtained solid was washed with ethyl acetate
  5. washwashed with saturated sodium bicarbonate solution and brine
  6. dry with materialThe organic portion was dried over anhydrous sodium sulfate
  7. concentrationconcentrated
  8. customThe obtained off-white solid was used without further purification (147, 0.864 g, 76%)

出典と根拠

ORDレコード
ord-3152bccee5844d5da8d704d660614213
出典データセット
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07872018B2

反応ノート

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