Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1857077Erstellt: 26. Oktober 2026

Oxygen → Adamantanone

https://huagongshe.com/reaction/1857077

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 64151—

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 60° C. in a sulfur dioxide (SO2) (0.5 atm) and oxygen (0.5 atm) atmosphere for 1 hour. A gas chromatographic analysis of a reaction mixture revealed that the conversion rate of adamantane was 91% and that a trace amount of 2-adamantanone was formed. 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 32%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06143924
Quelldatensatzuspto-grants-2000_11
ORD IDord-4471a22253394906bf076fdfba3146c1
Quellennotizuspto-grants-2000_11