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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2213972Generated: November 1, 2026

Phenylacetylene → 1-(3,3-Dimethyl-1-butyn-1-yl)-3-methoxybenzene

https://huagongshe.com/reaction/2213972

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetyleneHCID 10821—
Reactant3,3-Dimethyl-1-butyneHCID 13512—
Reactant3-MethoxybenzonitrileHCID 73712—
SolventBenzonitrileHCID 7505—
Product1-(3,3-Dimethyl-1-butyn-1-yl)-3-methoxybenzeneHCID 1146953392.5%

Reaction Steps

The procedure was identical to Example 1, with the exception that 3,3-dimethyl-1-butyne (0.488 ml; 0.329 g; 4.00 mmol) was used as a substrate instead of phenylacetylene and 3-methoxybenzonitrile (0.245 ml; 0.266 g; 2.00 mmol) was used as a substrate instead of benzonitrile. GC analysis of the organic phase of the hydrolyzed reaction sample after 16 h at 65° C. showed the presence of 1.85 mmol (92% yield) of 1-methoxy-3-(3,3-dimethyl-1-butynyl)benzene and no remaining 3-methoxybenzonitrile in the reaction mixture.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07105707B2
Source datasetuspto-grants-2006_09
ORD IDord-aef57bd0731b443c84b6528e143b28e3
Source noteuspto-grants-2006_09