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

HRID 908159
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HRID 908159 반응식
[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
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참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 962Water2회HCID 28259171-Methylsulfanyl-4-(2-nitro-propenyl)-benzene

생성물 1

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

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

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).

후처리

  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)

출처 및 근거

ORD 기록
ord-e81c0e31e91a46dabd7cab38492a80c4
출처 데이터셋
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08017608B2

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