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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 270985Generated: October 26, 2026

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

https://huagongshe.com/reaction/270985

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 numberUS07449533B2
Source datasetuspto-grants-2008_11
ORD IDord-cb5d1c826d7e47cb80af0dfe7127fa08
Source noteuspto-grants-2008_11