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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754394Generated: November 2, 2026

Triethylamine → HCID 86704449, compound

https://huagongshe.com/reaction/1754394

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAcryloyl chlorideHCID 13140—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 86704448HCID 86704448—
SolventDichloromethaneHCID 6344—
ProductHCID 86704449HCID 8670444980%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 5-allyl-2,2-dimethylpyrrolidine (1.5 g, 10.5 mmol) in 50 ml of anhydrous CH2Cl2, triethylamine (3 ml, 21 mmol) and acryloyl chloride (0.94 ml, 11.6 mmol) were added at 0° C. The reaction mixture was stirred at 0° C. for 1 hour and allowed to warm to room temperature and stirred for overnight. Analysis of the reaction mixture by LCMS indicated the completion of the reaction. Saturated aqueous NaHCO3 was added to the reaction mixture and the layers were separated. Aqueous layer was worked up twice with CH2Cl2 and the combined organic layers were dried over Na2SO4. Removal of the volatiles and purification of the crude by column chromatography gave the product in 80% yield (1.60 g) as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169249B2
Source datasetuspto-grants-2015_10
ORD IDord-52fd69b5555f47c2a3ce23153dda17e1
Source noteuspto-grants-2015_10