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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 271004Generated: October 30, 2026

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

https://huagongshe.com/reaction/271004

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantPyrrolidineHCID 31268—
ReactantHCID 22327806HCID 22327806—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
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 numberUS07449533B2
Source datasetuspto-grants-2008_11
ORD IDord-8030f6925cf34a5d9e2a7e5da8dd45bd
Source noteuspto-grants-2008_11