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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602846Generated: October 26, 2026

Hydrochloric Acid → 1-Methyl-3-(3,5-dimethyl-phenyl)-cyclopentadiene

https://huagongshe.com/reaction/602846

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-MethylcyclopentanoneHCID 14265—
ReactantBenzene, 1-bromo-3,5-dimethyl-HCID 136357—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
Product1-Methyl-3-(3,5-dimethyl-phenyl)-cyclopentadieneHCID 8662956946%

Reaction Steps

1-Bromo-3,5-dimethylbenzene (13.6 g, 73.6 mmol) was dissolved in a mixed solution of hexane (150 mL) and diethyl ether (20 mL) and added dropwise at 0° C. with a solution (46.6 mL, 1.58M) of n-butyllithium in hexane. The solution was immediately warmed to room temperature, stirred night and day and added dropwise at −78° C. to a solution of 3-methyl-2-cyclopentanone (7.3 mL, 74 mmol) in diethyl ether (100 mL). The resultant solution was warmed to room temperature immediately after dropwise addition and stirred for 2 hours. After termination of the reaction, the reaction solution was added with dilute hydrochloric acid, stirred at room temperature for 30 minutes and then subjected to layer separation. The organic layer was dried with magnesium sulfate and then had the solvent distilled off under reduced pressure. The crude product was distilled under reduced pressure (125 to 127° C./0.5 mmHg) to obtain 1-methyl-3-(3,5-dimethyl-phenyl)-cyclopentadiene (6.2 g, yield: 46%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07906599B2
Source datasetuspto-grants-2011_03
ORD IDord-d148eed8c1fb41e79daedb2f1b5153da
Source noteuspto-grants-2011_03