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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 63642Generated: October 25, 2026

Triphenylphosphine → N-Methyl-4-[(trimethylsilyl)ethynyl]aniline

https://huagongshe.com/reaction/63642

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantBenzenamine, 4-bromo-N-methyl-HCID 2757052—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
ProductN-Methyl-4-[(trimethylsilyl)ethynyl]anilineHCID 12387505937%

Reaction Steps

To a suspension of 4-bromo-N-methylaniline (500 mg, 2.7 mmol), trimethylsilyl acetylene (527 mg, 5.4 mmol), CuI (92 mg, 0.5 mmol) and PPh3 (233 mg, 0.9 mmol) in TEA (20 mL) was added PdCl2(PPh3)2 (94 mg, 0.1 mmol) at r.t. under N2. The reaction was stirred at reflux overnight. The reaction was filtered, concentrated, and purified by silica gel chromatography (PE:EtOAc=20:1) to give 200 mg (37%) of the title compound as a yellow oil. [M+H] Calc'd for C12H17NSi, 204. Found, 204.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447046B2
Source datasetuspto-grants-2016_09
ORD IDord-9b3f502c99cf41978d1aead30105a627
Source noteuspto-grants-2016_09