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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1090463Erstellt: 26. Oktober 2026

Benzoyl chloride → 9-Hydroxynonyl benzoate

https://huagongshe.com/reaction/1090463

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzoyl chlorideHCID 7412—
EduktTriethylamineHCID 8471—
Edukt1,9-NonanediolHCID 19835—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt9-Hydroxynonyl benzoateHCID 1991537454,4%

Reaktionsschritte

To a stirred solution of 51.2 grams (0.320 mole) of 1,9-nonanediol in 500 ml of tetrahydrofuran was added one crystal of p-dimethylaminopyridine, and then 8.9 grams (0.088 mole) of triethylamine was added. To this mixture was added dropwise a solution of 11.2 grams (0.08 mole) of benzoyl chloride in 40 ml of methylene chloride. Upon completion of addition, the reaction mixture was stirred at ambient temperature for 18 hours. The reaction mixture was concentrated under reduced pressure to a residue. The residue was dissolved in 200 ml of methylene chloride and was washed with five 75 ml portions of water. The organic layer was dried with magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure to a residue. Volatile materials were removed by distillation leaving 11.5 grams of 9-hydroxynonyl benzoate. The nmr spectrum was consistent with the proposed structure.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05081287
Quelldatensatzuspto-grants-1992_01
ORD IDord-306c48d83f8041f1aaf7d3ed00cf84fd
Quellennotizuspto-grants-1992_01