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Sulfuric Acid → 3-(1,3-Dioxaindan-5-yl)propane-1-thiol

HRID 486928
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 486928
[C:1](O)(=[S:3])[CH3:2].[O:5]1[C:16]2[C:8](=[CH:9][C:10](=[CH:14][CH:15]=2)[CH2:11]C=C)[O:7][CH2:6]1.[OH-].[Na+].S(=O)(=O)(O)O>C(O)C.O>[O:5]1[C:16]2[CH:15]=[CH:14][C:10]([CH2:11][CH2:2][CH2:1][SH:3])=[CH:9][C:8]=2[O:7][CH2:6]1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 1118Sulfuric AcidHCID 5144SafroleHCID 14798Sodium HydroxideHCID 178418634HCID 178418634, Verbindung

Produkt 1

HCID 190016193-(1,3-Dioxaindan-5-yl)propane-1-thiolAusbeute 66,4 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 702
Ethanol
Lösungsmittel
HCID 962WaterLösungsmittel

Versuchsvorschrift

25 g of thioacetic acid was added to 53.5 g of safrole in portions, while stirring the mixture at a room temperature or under cooling with ice/water. The reaction was carried out for 30 minutes. A solution of 20 g of sodium hydroxide in a mixture comprising 100 ml of water and 200 ml of ethanol was added to the reaction mixture. The obtained mixture was heated under reflux for 20 minutes, cooled, neutralized with dilute sulfuric acid and extracted with 1 l of benzene. The extract was washed with water and the benzene layer was dried over anhydrous sodium sulfate and purified by silica gel column chromatography (hexane) to obtain 42.8 g of the title compound as a colorless oil.

Aufarbeitung

  1. temperatureThe obtained mixture was heated
  2. temperatureunder reflux for 20 minutes
  3. temperaturecooled
  4. extractionextracted with 1 l of benzene
  5. washThe extract was washed with water
  6. dry with materialthe benzene layer was dried over anhydrous sodium sulfate
  7. custompurified by silica gel column chromatography (hexane)

Quellen und Nachweise

ORD-Eintrag
ord-bc49ae4e5efa440f81f3746c1ac1f30b
Quelldatensatz
uspto-grants-1994_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05292901

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