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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2194325Generated: November 3, 2026

Triethylamine → 9H-Fluoren-9-YL acrylate

https://huagongshe.com/reaction/2194325

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAcryloyl chlorideHCID 13140—
ReactantFluoren-9-olHCID 74318—
SolventBenzeneHCID 241—
Product9H-Fluoren-9-YL acrylateHCID 5793157273%

Reaction Conditions

Temperature8 °C

Reaction Steps

To a 250 mL round-bottomed flask was added 9-hydroxyfluorene (5 g, 27.4 mmol) and triethylamine (3.86 ml, 27.4 mmol) in benzene (150 mL) to give a colorless solution. The solution was cooled to 8° C. with an ice bath. Next, acryloyl chloride (2.229 mL, 27.4 mmol) was dissolved in 25 mL of benzene, placed in a dropping funnel, and added over 1 hour with vigorous stirring. The reaction formed a white precipitate. The ice bath was removed and the viscous sludge was stirred overnight at room temperature. The resulting cloudy white suspension was washed with 50 mL water, followed by 50 mL 5% NaOH solution, and 50 mL water. The benzene layer was collected and dried with MgSO4, filtered, and rotovapped to give the 9-fluorenylacrylate as a viscous beige oil which crystallized on cooling to 4° C. (4.73 g, 20.02 mmol, 73.0% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08334026B2
Source datasetuspto-grants-2012_12
ORD IDord-31841909e770484fbd5e10ccd5d213ec
Source noteuspto-grants-2012_12