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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058158Generated: October 26, 2026

Dichloromethane → 3-(1,3-Dioxan-2-yl)-1-(5-norbornen-2-yl)-1-propyl acetate

https://huagongshe.com/reaction/1058158

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
Reactant3-(1,3-Dioxan-2-yl)-1-(5-norbornen-2-yl)-1-propanolHCID 22281037—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventWaterHCID 962—
Product3-(1,3-Dioxan-2-yl)-1-(5-norbornen-2-yl)-1-propyl acetateHCID 2228103696%

Reaction Steps

To a mixture of 15.0 g of 3-(1,3-dioxan-2-yl)-1-(5-norbornen-2-yl)-1-propanol, 9.6 g of acetic anhydride, 100 mg of 4-dimethylaminopyridine and 50 ml of methylene chloride, 10.2 g of triethylamine was added dropwise over 30 minutes at 20° C. Stirring was continued for 30 minutes whereupon 10 g of water was added to stop reaction. Stirring was continued for a further 30 minutes whereupon water was added to the reaction solution, which was extracted with hexane. The organic layer was successively washed with water and saturated sodium chloride water, dried over anhydrous sodium sulfate, and concentrated in vacuum. It was further purified by vacuum distillation, obtaining 16.9 g of 3-(1,3-dioxan-2-yl)-1-(5-norbornen-2-yl)-1-propyl acetate (boiling point 125° C./53 Pa, yield 96%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06515149B2
Source datasetuspto-grants-2003_02
ORD IDord-dd5c674685b143a39c63bb57473b74bf
Source noteuspto-grants-2003_02