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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 495745Generated: October 30, 2026

Acetone → 3-(1,1,3-Trimethylbutyl)-6,6-dimethylfulvene

https://huagongshe.com/reaction/495745

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantDiethyl EtherHCID 3283—
ReactantPyrrolidineHCID 31268—
ReactantHCID 22327806HCID 22327806—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product3-(1,1,3-Trimethylbutyl)-6,6-dimethylfulveneHCID 2232777794%

Reaction Steps

To a solution of 3.00 g (18.3 mmol) of (1,1,3-trimethylbutyl)cyclopentadiene in 30 ml of methanol, 13.4 ml (182.5 mmol) of acetone and 3.1 ml (36.6 mmol) of pyrrolidine were added with ice cooling, followed by stirring at room temperature for one night. After the reaction solution was diluted with % 100 ml of ether, 50 ml of water was added. The organic phase was separated, washed with water and a saturated saline solution, then dried over anhydrous magnesium sulfate and filtered. From the filtrate, the solvent was removed under reduced pressure to obtain a liquid. The liquid was subjected to vacuum distillation (130° C./1 mmHg) to obtain 3.50 g (17.1 mmol) of a yellow liquid (yield: 94%). The analyzed values are given below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06939928B1
Source datasetuspto-grants-2005_09
ORD IDord-71697aff8bd043429b19e750e4aed7fa
Source noteuspto-grants-2005_09