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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2260928Generated: October 25, 2026

Sulfuric Acid → 3-Methylcyclopentadecene-1-yl acetate

https://huagongshe.com/reaction/2260928

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantAcetic AnhydrideHCID 7918—
ReactantTriphenyl PhosphateHCID 8289—
Reactant2-CyclopentadecenoneHCID 54040345—
ReactantHCID 178477796HCID 178477796—
Catalystcopper(II) trifluoromethanesulfonateHCID 2734996—
SolventTolueneHCID 1140—
Product3-Methylcyclopentadecene-1-yl acetateHCID 6877537292%

Reaction Conditions

Temperature25 °C

Reaction Steps

Placed in a 2000-mL flask equipped with a stirrer, dropping funnel and thermometer were 54.3 mg (0.15 mmol) of Cu(OTf)2, 25 g of toluene and 93.1 mg (0.30 mmol) of triphenyl phosphate, and the inner atmosphere was replaced with nitrogen. After replacement with nitrogen, the mixture was stirred at 25° C. for 20 min. Then, 9 mL (18 mmol) of a toluene solution (2.0 mmol/L) of dimethylzinc was added to the mixture at 25° C., followed by further stirring for 10 min. The mixture was then cooled to −17° C., followed by addition of 1.68 g (16.5 mmol) of acetic anhydride, and 3.34 g (15 mmol) of 2-cyclopentadecenone was added dropwise to the mixture over the period of 1 hour. After completion of the dropwise addition, stirring was continued at the same temperature for 6 hours. After the reaction was completed, 32.5 g of a 5% aqueous sulfuric acid solution as cooled to 0° C. was added to the reaction mixture for quenching. After separation, the organic layer was washed with water (5 times), and the resultant organic layer was concentrated under reduced pressure to give 4.93 g of a crude product. The crude product was purified by silica-gel column chromatography to produce 3.89 g (13.8 mmol, 92% yield) of dl-3-methycyclopentadecene-1-yl acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07846701B2
Source datasetuspto-grants-2010_12
ORD IDord-795cf151034845a4ac043124c056d6c5
Source noteuspto-grants-2010_12