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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 726835Generated: October 31, 2026

Acetone → HCID 19606731, compound

https://huagongshe.com/reaction/726835

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantPyrrolidineHCID 31268—
ReactantHCID 131720401HCID 131720401—
SolventMethanolHCID 887—
ProductHCID 19606731HCID 1960673188%

Reaction Conditions

Temperature0 °C

Reaction Steps

7.70 g (34.0 mmol) of the cyclopentadienyltetrahydroindene (Example 5) are dissolved in 70 ml of methanol and cooled to 0° C. The orange-red reaction solution is subsequently treated successively with 2.96 g (51.0 mmol) of acetone and 4.83 g (68.0 mmol) of pyrrolidine. The mixture is stirred at 0° C. for 5 hours and then, in order to complete the reaction, at room temperature for a further 2 hours, before the reaction is terminated by addition of 4 ml of glacial acetic acid. The red, clear reaction solution is hydrolyzed by means of 200 ml of water, and the yellow suspension is extracted 3× with 50 ml of diethyl ether in each case. Repeated washing of the combined organic phases with saturated, aqueous sodium chloride solution and drying over magnesium sulfate give the fulvene as an orange-red, wax-like residue in a yield of 88% (8.00 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05710297
Source datasetuspto-grants-1998_01
ORD IDord-62ea0cdae4364e749c552df386d23766
Source noteuspto-grants-1998_01