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Hydrochloric Acid → 1-[4-(Methylsulfanyl)phenyl]propan-2-one

HRID 908159
ノート
印刷プレビュー

反応式

HRID 908159 の反応式
[CH3:1][S:2][C:3]1[CH:8]=[CH:7][C:6]([CH:9]=[C:10]([N+]([O-])=O)[CH3:11])=[CH:5][CH:4]=1.Cl.[OH2:16]>C(Cl)(Cl)Cl>[CH3:1][S:2][C:3]1[CH:8]=[CH:7][C:6]([CH2:9][C:10](=[O:16])[CH3:11])=[CH:5][CH:4]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 313Hydrochloric AcidHCID 962Water2 回HCID 28259171-Methylsulfanyl-4-(2-nitro-propenyl)-benzene

生成物 1

HCID 134577081-[4-(Methylsulfanyl)phenyl]propan-2-one

試薬・触媒・溶媒 1

HCID 6212Chloroform溶媒

実験手順

A stirred mixture of crude 1-methylsulfanyl-4-(2-nitro-propenyl)-benzene (27a) (28.8 mmol) iron filings (6.25 g, 112 mmol) and ferric chloride hexahydrate (0.155 g, 0.57 mmol) in water (20 ml) is heated to reflux. Concentrated hydrochloric acid (10 ml) is added over 2 hours the reflux continued for 4 hours. After 18 hours at room temperature the reaction is diluted with water and chloroform. The mixture is filtered through celite and the organic extract is separated. The aqueous extract is extracted with chloroform and the combined organic extracts are dried (MgSO4). The solvent is removed and the residue is purified by chromatography on silica eluting with hexane-ethyl acetate (3:1) to afford the title compound (2.65 g).

後処理

  1. temperatureis heated to reflux
  2. filtrationThe mixture is filtered through celite
  3. extractionthe organic extract
  4. customis separated
  5. extractionThe aqueous extract
  6. extractionis extracted with chloroform
  7. dry with materialthe combined organic extracts are dried (MgSO4)
  8. customThe solvent is removed
  9. customthe residue is purified by chromatography on silica eluting with hexane-ethyl acetate (3:1)

出典と根拠

ORDレコード
ord-e81c0e31e91a46dabd7cab38492a80c4
出典データセット
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08017608B2

反応ノート

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