Sulfuric Acid → Propanoic acid, 2-chloro, 3-butenyl ester

HRID 2308041

Reaktionsgleichung

Reaktionsgleichung von HRID 2308041
[CH3:1][CH:2]([C:4]([OH:6])=[O:5])[Cl:3].[CH2:7]=[CH:8][CH2:9][CH2:10]O.S(=O)(=O)(O)O.C(=O)([O-])[O-].[Na+].[Na+]>COC(C)(C)C.O>[CH3:1][CH:2]([C:4]([O:6][CH2:10][CH2:9][CH:8]=[CH2:7])=[O:5])[Cl:3]

Komponenten

7

Versuchsvorschrift

CH3CHClCOOH (50 g)and CH2═CH(CH2)2OH (75 ml) were put into a flask and stirred and 10 ml of concentrated sulfuric acid was added dropwise thereto over period of 10 minutes at room temperature. The resulting reaction solution was added to 250 ml of a saturated sodium carbonate aqueous solution. Water (150 ml) and tert-butyl methyl ether (150 ml) were added thereto, followed by liquid separation to obtain a tert-butyl methyl ether layer as an organic layer. Further, the organic layer was washed with 150 ml of water, dried over magnesium sulfate and then subjected to filtration to obtain a crude liquid. The crude liquid was concentrated to obtain CH3CHClCOO(CH2)2CH═CH2.

Aufarbeitung

  1. customThe resulting reaction solution
  2. customfollowed by liquid separation
  3. customto obtain a tert-butyl methyl ether layer as an organic layer
  4. washFurther, the organic layer was washed with 150 ml of water
  5. dry with materialdried over magnesium sulfate
  6. filtrationsubjected to filtration
  7. customto obtain a crude liquid
  8. concentrationThe crude liquid was concentrated

Quellen und Nachweise

ORD-Eintrag
ord-bc4cb01ca8914cad9e3a661b74562c42
Quelldatensatz
uspto-grants-2004_12
Patentnummer
US06833477B2

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