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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2399601Generated: October 31, 2026

Pyridine → 1-Penten-3-yl Acetate

https://huagongshe.com/reaction/2399601

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetic AnhydrideHCID 7918—
Reactant1-PenteneHCID 8004—
SolventDiethyl EtherHCID 3283—
Product1-Penten-3-yl AcetateHCID 530323—

Reaction Steps

The above pentene derivative (9.0 g, 25 mmols) and acetic anhydride (3.0 g, 30 mmols) are dissolved in ether (200 ml), followed by dropwise adding pyridine (5 ml), while stirring the solution under ice cooling, stirring the reaction liquid under ice cooling for one hour, elevating the temperature up to room temperature, stirring for 3 hours, pouring the reaction mixture into ice water after completion of the reaction, extracting with toluene (150 ml), washing the organic layer with water, drying over anhydrous magnesium sulfate and concentrating under reduced pressure to obtain 5-(4-(4-propylphenyl)phenyl)cyclohexyl)-3-acetyloxy-1-pentene pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05449810
Source datasetuspto-grants-1995_09
ORD IDord-3c3ae2aeb27a498d8f9b2159de3a625a
Source noteuspto-grants-1995_09