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Dichloromethane → HCID 17764601、化合物

HRID 1004171
ノート
印刷プレビュー

反応式

HRID 1004171 の反応式
[Cl:1][C:2]1[S:3][C:4](Cl)=[CH:5][C:6]=1[CH3:7].C[O:10]C(Cl)Cl.[CH2:14]([Cl:16])Cl>>[Cl:1][C:2]1[S:3][C:14]([Cl:16])=[C:5]([CH3:4])[C:6]=1[CH:7]=[O:10]
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 6344DichloromethaneHCID 21004Methane, dichloromethoxy-HCID 2689102,5-Dichloro-3-methylthiophene

生成物 1

HCID 17764601HCID 17764601、化合物

実験手順

To a stirred solution of 2,5-dichloro-3-methylthiophene [prepared according to the method of J. Amer. Chim. Soc., 1971, 333.] (11.8 g) in CH2Cl2 (200 mL) was added TiCL1 (37.94 g) and dichloromethyl methyl ether (12.6 g) at -10° C. After stirring for 4 hours, the reaction mixture was poured into ice-water and the whole was stirred vigorously for 30 minutes. The resulting mixture was extracted with CH2Cl2 (200 ml×1), and the organic layers was washed with saturated NaHCO3 solution(100 mL×1), brine (100 mL×1), dried over MgSO4, and concentrated in vacuo. The resulting residue was purified by distillation (bp : 140-145° C./10 mmHg) to provide the subtitle compound (11.75 g).

後処理

  1. stirringthe whole was stirred vigorously for 30 minutes
  2. extractionThe resulting mixture was extracted with CH2Cl2 (200 ml×1)
  3. washthe organic layers was washed with saturated NaHCO3 solution(100 mL×1), brine (100 mL×1)
  4. dry with materialdried over MgSO4
  5. concentrationconcentrated in vacuo
  6. distillationThe resulting residue was purified by distillation (bp : 140-145° C./10 mmHg)

出典と根拠

ORDレコード
ord-134e32f3ba1241f7b750fa4201790f11
出典データセット
uspto-grants-2000_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06048880

反応ノート

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