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Sulfuric Acid → 2-[[Bis(allyloxy)phosphoryl]oxymethyl]-3-methoxybenzoic acid

HRID 1766911
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1766911
[P:1]([O:11][CH2:12][C:13]1[C:18]([O:19][CH3:20])=[CH:17][CH:16]=[CH:15][C:14]=1[CH2:21][OH:22])([O:7][CH2:8][CH:9]=[CH2:10])([O:3][CH2:4][CH:5]=[CH2:6])=[O:2].[Cr](O[Cr]([O-])(=O)=O)([O-])(=O)=[O:24].[NH+]1C=CC=CC=1.[NH+]1C=CC=CC=1.CC(C)=O.OS(O)(=O)=O.O=[Cr](=O)=O.S(=O)(=O)(O)O>CN(C)C=O.CC(C)=O.O.CC(O)C>[CH2:4]([O:3][P:1]([O:11][CH2:12][C:13]1[C:18]([O:19][CH3:20])=[CH:17][CH:16]=[CH:15][C:14]=1[C:21]([OH:24])=[O:22])([O:7][CH2:8][CH:9]=[CH2:10])=[O:2])[CH:5]=[CH2:6]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

9

Edukt 4

HCID 1118Sulfuric AcidHCID 2724130Cornforth reagentHCID 17862616Diallyl 2-(hydroxymethyl)-6-methoxybenzyl phosphateHCID 131709961Jones' reagent

Produkt 1

HCID 178625362-[[Bis(allyloxy)phosphoryl]oxymethyl]-3-methoxybenzoic acidAusbeute 60 %

Reagenzien, Katalysatoren, Lösungsmittel 4

HCID 180AcetoneLösungsmittel
HCID 962WaterLösungsmittel2×
HCID 3776IsopropanolLösungsmittel
HCID 6228DimethylformamideLösungsmittel

Versuchsvorschrift

Diallyl 2-(hydroxymethyl)-6-methoxybenzyl phosphate (715.0 mg, 2.18 mmol) obtained from Example 21-(4) was dissolved in N,N-dimethylformamide (8 ml), and pyridinium dichromate (2.87 g, 7.63 mmol) was added thereto. After the mixture was stirred at room temperature for 12 hours, water (60 ml) was added thereto, and the product was extracted with diethyl ether. The organic layer was washed successively with water, a 2N aqueous solution of hydrochloric acid, and a saturated aqueous solution of sodium chloride, and then the solvent was distilled off under reduced pressure to give an oily residue. The residue was dissolved in acetone (5 ml), and Jones reagent (a mixture of chromic anhydride (5.34 g, 4 mmol) and concentrated sulfuric acid (4.6 ml) diluted with water to 20 ml total volume; 1.5 ml) was added thereto. The reaction mixture was stirred at room temperature for 1.5 hours, and then 2-propanol (1 ml) was added thereto to stop the reaction. The solid insoluble material was filtered off, and the filtrate was concentrated under reduced pressure to give an oily residue. The residue was dried using a vaccum pump, and then subjected to chromatography on a silica gel (25 g) column (eluent; ethyl acetate:dichloromethane=1:1) to afford the title compound (447.0 mg, 60% yield) as a colorless oil.

Aufarbeitung

  1. extractionthe product was extracted with diethyl ether
  2. washThe organic layer was washed successively with water
  3. distillationa 2N aqueous solution of hydrochloric acid, and a saturated aqueous solution of sodium chloride, and then the solvent was distilled off under reduced pressure
  4. customto give an oily residue
  5. additionwas added
  6. stirringThe reaction mixture was stirred at room temperature for 1.5 hours
  7. customthe reaction
  8. filtrationThe solid insoluble material was filtered off
  9. concentrationthe filtrate was concentrated under reduced pressure
  10. customto give an oily residue
  11. customThe residue was dried

Quellen und Nachweise

ORD-Eintrag
ord-a9ca631527d34189afbe6ba459b44a5e
Quelldatensatz
uspto-grants-2007_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07230023B2

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