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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606815Generated: October 31, 2026

Triethylamine → N-(2-Fluoro-5-trimethylsilanylethynylbenzyl)-methanesulfonamide

https://huagongshe.com/reaction/606815

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantN-(5-bromo-2-fluorobenzyl)methanesulfonamideHCID 40161431—
CatalystZinc bromideHCID 10421208—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
ProductN-(2-Fluoro-5-trimethylsilanylethynylbenzyl)-methanesulfonamideHCID 6704754174%

Reaction Conditions

Temperature60 °C

Reaction Steps

Dissolve zinc (II) bromide (313 mg, 1.20 mmol) in tetrahydrofuran (2.5 mL) and treat with triethylamine (0.64 mL, 4.80 mmol). After 4 min add N-(5-bromo-2-fluorobenzyl)methanesulfonamide (282 mg, 1.00 mmol), (prepared as described in PREPARATION 35), trimethylsilylacetylene (0.30 mL, 2.12 mmol), and tetrakis(triphenylphosphine)palladium (0) (58 mg, 0.050 mmol) to the reddish solution. Heat to 60° C. in a sealed tube overnight, cool to room temperature and filter through diatomaceous earth with ethyl acetate. Concentrate the filtrate and purify the residue by silica gel chromatography, eluting with 75:25 hexanes:ethyl acetate, to give the title compound as a white crystalline solid (220 mg, 74%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915424B2
Source datasetuspto-grants-2011_03
ORD IDord-d2f92a028c4849448d327706acd8e3fe
Source noteuspto-grants-2011_03