3-Aminophenylacetylene
[CAS# 54060-30-9]

Identification

• Classification: Pharmaceutical intermediate >> API intermediate
• Name: 3-Aminophenylacetylene
• Synonyms: 3-Ethynylaniline
• Molecular Formula: C₈H₇N
• Molecular Weight: 117.15
• CAS Registry Number: 54060-30-9
• EC Number: 258-944-6
• SMILES: C#CC1=CC(=CC=C1)N

Properties

• Density: 1.1±0.1 g/cm³ Calc.^*, 1.12 g/mL (Expl.)
• Melting point: 27 ºC (Expl.)
• Boiling point: 240.5±23.0 ºC 760 mmHg (Calc.)^*, 282.3 ºC (Expl.)
• Flash point: 111.0±17.9 ºC (Calc.)^*, 59 ºC (Expl.)
• Index of refraction: 1.59 (Calc.)^*, 1.617 (Expl.)

^* Calculated using Advanced Chemistry Development (ACD/Labs) Software.

Safety Data

• Hazard Symbols: GHS02;GHS07 WarningGHS02
• Hazard Statements: H226-H315-H319-H335
• Precautionary Statements: P210-P233-P240-P241-P242-P243-P261-P264-P264+P265-P271-P280-P302+P352-P303+P361+P353-P304+P340-P305+P351+P338-P319-P321-P332+P317-P337+P317-P362+P364-P370+P378-P403+P233-P403+P235-P405-P501

Hazard Classification

Hazard	Class	Category Code	Hazard Statement
Skin irritation	Skin Irrit.	2	H315
Eye irritation	Eye Irrit.	2	H319
Specific target organ toxicity - single exposure	STOT SE	3	H335
Flammable liquids	Flam. Liq.	3	H226
Acute toxicity	Acute Tox.	4	H332
Acute toxicity	Acute Tox.	4	H312
Acute toxicity	Acute Tox.	4	H302
Eye irritation	Eye Irrit.	2A	H319

• Transport Information: UN 1993

Discovory and Applicatios

3-Aminophenylacetylene is an organic compound consisting of a phenyl ring substituted with an amino group at the meta-position (position 3) and an ethynyl group (-C≡CH) directly bonded to the ring. Its molecular structure can be described as a derivative of phenylacetylene, where the amine substituent is introduced at the 3-position, resulting in a compound with both nucleophilic and electrophilic reactive sites.

The synthesis of 3-aminophenylacetylene typically involves functional group transformation of 3-nitrophenylacetylene, where the nitro group is reduced to a primary amine using standard reducing agents such as palladium on carbon with hydrogen, or by chemical reduction with tin(II) chloride or iron in acidic conditions. The acetylene group, being terminal and relatively reactive, allows for straightforward synthetic modifications, such as Sonogashira couplings, cycloadditions, or coordination to metal centers.

3-Aminophenylacetylene is of interest in various areas of chemical research, especially in the synthesis of conjugated systems and functional materials. The ethynyl group provides a linear extension to the aromatic system, enabling the formation of extended π-conjugated frameworks useful in the design of organic electronic materials, such as conductive polymers, light-emitting diodes, and photovoltaic materials. The amino group, being electron-donating, can influence the electronic properties of the molecule, making it suitable for tuning charge transport or light absorption characteristics.

In the field of medicinal chemistry, aromatic acetylenes bearing amino groups have been studied as building blocks for the development of kinase inhibitors, enzyme modulators, and bioactive heterocycles. The ethynyl group serves as a versatile handle for further chemical elaboration, including the formation of heteroaromatic systems such as indoles or triazoles, especially through cycloaddition reactions like the Huisgen 1,3-dipolar cycloaddition. Additionally, the amino group can participate in hydrogen bonding or serve as a site for conjugation to larger biomolecules or polymers.

The dual reactivity of 3-aminophenylacetylene allows it to serve as a bifunctional monomer in polymer chemistry. It can undergo polymerization reactions involving either the amino or ethynyl groups, leading to materials with diverse mechanical and optical properties. This makes it a valuable component in the design of specialty polymers, adhesives, or coatings with tailored performance characteristics.

Analytically, derivatives of 3-aminophenylacetylene are used as intermediates in the synthesis of fluorescent dyes or molecular probes. The rigid and planar structure formed by conjugated systems containing phenylacetylene moieties allows for strong fluorescence and favorable binding to biomolecules. The amine functionality facilitates derivatization with fluorophores, chelators, or affinity tags.

In coordination chemistry, the ethynyl group of 3-aminophenylacetylene can bind to transition metal centers, forming stable complexes that exhibit interesting catalytic or electronic behavior. Such complexes have been explored in organometallic catalysis, where the acetylene moiety interacts with metals such as palladium, platinum, or ruthenium, and the amino group modulates the electronic environment of the complex.

The presence of both amino and ethynyl substituents in a single molecule makes 3-aminophenylacetylene a synthetically flexible and functionally rich intermediate, suitable for the development of new materials, biologically active molecules, and organometallic compounds across multiple scientific disciplines.

References

2016. Facile strategy for preparation of alkyne-functionalized cellulose fibers with click reactivity. Cellulose, 24(2).
DOI: 10.1007/s10570-016-1153-1

2018. Ribosome-Templated Azide�Alkyne Cycloadditions Using Resistant Bacteria as Reaction Vessels: in Cellulo Click Chemistry. ACS Medicinal Chemistry Letters, 9(9).
DOI: 10.1021/acsmedchemlett.8b00248

2024. Synthesis and antitumor activity of dolutegravir derivatives bearing 1,2,3-triazole moieties. BMC Chemistry, 18(1).
DOI: 10.1186/s13065-024-01205-3