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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2213973Generated: November 1, 2026

Phenylacetylene → HCID 11367272, compound

https://huagongshe.com/reaction/2213973

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetyleneHCID 10821—
Reactant3,3-Dimethyl-1-butyneHCID 13512—
Reactant3-AminobenzonitrileHCID 16702—
SolventBenzonitrileHCID 7505—
ProductHCID 11367272HCID 1136727248%

Reaction Steps

The procedure was identical to Example 2, 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-aminobenzonitrile (0.236 g; 2.00 mmol) was used as a substrate instead of benzonitrile. GC analysis of the organic phase of the hydrolyzed reaction sample after 45 h at 65° C. showed the presence of 0.96 mmol (48% yield) of 1-amino-3-(3,3-dimethyl-1-butynyl)benzene and 1.00 mmol of 3-aminobenzonitrile remaining in the reaction mixture.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07105707B2
Source datasetuspto-grants-2006_09
ORD IDord-51bb9d7c6d1e4a549bd83cf44d153143
Source noteuspto-grants-2006_09