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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1857078Erstellt: 26. Oktober 2026

Oxygen → Adamantanone

https://huagongshe.com/reaction/1857078

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktOxygenHCID 977—
EduktSulfur DioxideHCID 1119—
EduktAdamantaneHCID 9238—
EduktN-HydroxyphthalimideHCID 10665—
KatalysatorSodium orthovanadateHCID 61671—
KatalysatorBis(2,4-pentanedionato)vanadium(IV) OxideHCID 16217092—
LösungsmittelAcetic AcidHCID 176—
ProduktAdamantanoneHCID 641517%

Reaktionsschritte

A mixture of 2 mmol of adamantane, 0.2 mmol of N-hydroxyphthalimide, 0.01 mmol of vanadyl acetylacetonato [(VO (acac) 2 ], and 5 ml of acetic acid was stirred at 40° C. in a sulfur dioxide (SO2) (0.5 atm) and oxygen (0.5 atm) atmosphere for 2 hours. A gas chromatographic analysis of a reaction mixture revealed that the conversion rate of adamantane was 63% and that 2-adamantanone was formed in a yield of 7%. The reaction mixture was extracted with water, was neutralized with an aqueous sodium hydroxide solution, and was adjusted to weak acidity with hydrochloric acid. An aqueous benzyl isothiourea hydrochloride solution in large excess was then added to the mixture to separate S-benzyl thiuronium salt of 1-adamantanesulfonic acid. The yield of this compound was 40%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06143924
Quelldatensatzuspto-grants-2000_11
ORD IDord-3f489a5ad76a491f817617e255042899
Quellennotizuspto-grants-2000_11