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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 992592Generated: November 1, 2026

Phenylacetylene → Benzene, 1-ethynyl-2-(phenylethynyl)-

https://huagongshe.com/reaction/992592

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetyleneHCID 10821—
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant1-BROMO-2-PHENYLETHYNYL-BENZENEHCID 11032519—
ProductBenzene, 1-ethynyl-2-(phenylethynyl)-HCID 11769569—

Reaction Steps

In an especially contemplated arm extension strategy depicted in FIG. 4, in which AD represents an adamantane or diamantane group. Phenylacetylene is a starting molecule that is reacted (A1) with TBA (supra) to yield tetrakis(mono-tolanyl)-adamantane. Alternatively, phenylacetylene can be converted (B1) to tolanylbromide that is subsequently reacted (C1) with trimethylsilylacetylene to form tolanylacetylene. TBA can then be reacted (A2) with tolanylacetylene to tetrakis(bistolanyl )-adamantane. In a further extension reaction, tolanylacetylene is reacted (B2) with 1-bromo-4-iodobenzene to bistolanylbromide that is further converted (C2) to bistolanylacetylene. The so formed bistolanylacetylene may then be reacted (A3) with TBA to yield tetrakis(tristolanyl)-adamantane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06469123B1
Source datasetuspto-grants-2002_10
ORD IDord-6774e58e9b5a4bc59ced7ad3912cdb2e
Source noteuspto-grants-2002_10