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Potassium Hydroxide → Hydrogenmaleate

HRID 380345
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 380345
C1(SC2C=CC=C[C:9]=2[C:10](O)=[O:11])C=CC=CC=1.[OH-:17].[K+].[C:19]([OH:26])(=[O:25])/[CH:20]=[CH:21]\[C:22]([OH:24])=[O:23]>O.C(O)C>[CH2:10]([OH:11])[CH2:9][O:23][C:22]([CH2:21][CH:20]([OH:17])[C:19]([OH:26])=[O:25])=[O:24]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 14797Potassium HydroxideHCID 152102-(Phenylthio)benzoic acidHCID 444266Maleic Acid

Produkt 1

HCID 87460142HydrogenmaleateAusbeute 90,2 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 702EthanolLösungsmittel2×HCID 962
Water
Lösungsmittel

Reaktionsbedingungen

Temperatur
20 °C

Versuchsvorschrift

A mixture of methyl 2-(4-(2-chloroethoxy)phenylsulfanyl)benzoate (7.2 g, 22.0 mmol), 1-(4-chlorobenzyl)piperazine (4.6 g, 22.0 mmol), anhydrous potassium carbonate (10.5 g), potassium iodide (0.2 g) and 4-methylpentane-2-one (120 ml) was refluxed for 20 h (the reaction was monitored by TLC and continued till 1-(4-chlorobenzyl)piperazine was not present in the reaction mixture). The hot mixture was filtered, the filtrate was evaporated to dryness. The residue was purified by column chromatography on silica gel using dichloromethane and chloroform as eluents. Crystallization from a mixture of n-hexane-ether (1:1) provided methyl ester of the title acid (4.2 g, 38.5%), m.p. 106-108° C. For C27H29ClN2O3S (497.1) calculated: 65.24% C, 5.88% H, 7.13% Cl, 5.64% N, 6.45% S; found: 65.62% C, 6.19% H, 7.08% Cl, 5.20% N, 6.35% S. 1H NMR spectrum (CDCl3): CH3(ester) 3.96 s; aromatic H on the phenylsulfanylbenzoic acid moiety: H(6) 8.00 dd (J=2.0, 7.5 Hz); H(3,4,5,3′,5′) 6.68-7.20 m; aromatic H of 4-chlorobenzyl group 7.28 s. A solution of potassium hydroxide (1.7 g) in water (10 ml) was added to a stirred solution of this ester (3.7 g, 7.4 mmol) in ethanol (40 ml) and the mixture was refluxed for 1 h. The residue after evaporation was dissolved in water and acidified with acetic acid, the mixture was cooled down and the formed precipitate was extracted with chloroform. The extract was dried with sodium sulfate, the residue after evaporation was suspended in ethanol (50 ml) and a solution of maleic acid (1.2 g, 10.0 mmol) in ethanol (10 ml) was added and the mixture was stirred for 8 h at 20° C. The insoluble portion was filtered off, washed with ethanol to provide the title hydrogenmaleate (4.0 g, 90.2%), m.p. 194-196 ° C. For C26H27ClN2O3S. C4H4O4 (599.1) calculated: 60.14% C, 5.22% H, 5.92% Cl, 4.68% N, 5.35% S; found: 59.94% C, 5.31% H, 6.01% Cl, 4.51% N,5.26% S.

Aufarbeitung

  1. customaromatic H of 4-chlorobenzyl group 7.28 s
  2. temperaturethe mixture was refluxed for 1 h
  3. customThe residue after evaporation
  4. dissolutionwas dissolved in water
  5. temperaturethe mixture was cooled down
  6. extractionthe formed precipitate was extracted with chloroform
  7. dry with materialThe extract was dried with sodium sulfate
  8. customthe residue after evaporation
  9. filtrationThe insoluble portion was filtered off
  10. washwashed with ethanol

Quellen und Nachweise

ORD-Eintrag
ord-77117672f60642cb954889c398b1b8a5
Quelldatensatz
uspto-grants-2001_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06303612B1

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