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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1242863Generated: October 30, 2026

Gamma-Butyrolactone → 1(2H)-Naphthalenone, 3,4-dihydro-5,8-dimethyl-

https://huagongshe.com/reaction/1242863

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGamma-ButyrolactoneHCID 7302—
ReactantP-XyleneHCID 7809—
Product1(2H)-Naphthalenone, 3,4-dihydro-5,8-dimethyl-HCID 9933428.7%

Reaction Steps

After the completion of the first reaction in Example 1, the supernatant was removed, the remained catalyst was washed with 100 ml of hexane with stirring at room temperature. The hexane supernatant was removed, followed by drying under reduced pressure at 50° C. 100 ml of p-xylene (799 mmol) and 1 ml of γ-butyrolactone (14.8 mmol) as raw materials were charged again and then reacted at 196° C. for 3 hours. As a result, 5,8-dimethyltetralone (yield based on γ-butyrolactone: 28.7%) was obtained. The effect of regenerating the catalyst was exerted.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115782B2
Source datasetuspto-grants-2006_10
ORD IDord-e6392f534cc04a71948ac52fd4d6aa3c
Source noteuspto-grants-2006_10