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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 495726Generated: October 26, 2026

Acetone → 2-tert-Butyl-5-(propan-2-ylidene)cyclopenta-1,3-diene

https://huagongshe.com/reaction/495726

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantMethanolHCID 887—
ReactantPyrrolidineHCID 31268—
ReactantTert-butylcyclopentadieneHCID 633714—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product2-tert-Butyl-5-(propan-2-ylidene)cyclopenta-1,3-dieneHCID 1468828390.8%

Reaction Steps

To a mixed solution of 1.40 g (11 mmol) of tert-butylcyclopentadiene, 8.4 ml (114 mmol) of acetone and 20 ml of methanol, 9.5 ml (114 mmol) of pyrrolidine was added with ice cooling, followed by stirring at room temperature for one night. To the reaction solution, 50 ml of water, 100 ml of ether and 3 ml of acetic acid were added with ice cooling. The separated organic phase was washed with water and dried over anhydrous sodium sulfate. After the solvent was distilled off, the residue was subjected to column chromatography (silica gel, developing solvent: hexane) to obtain 1.62 g of a yellow liquid (yield: 88%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06939928B1
Source datasetuspto-grants-2005_09
ORD IDord-fe5bfe36c43045fc8249f5c4ac3cd36a
Source noteuspto-grants-2005_09