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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 427242Generated: October 31, 2026

Sodium Chloride → methyl N-[2-fluoro-5-(trimethylsilylethynyl)benzyl]carbamate

https://huagongshe.com/reaction/427242

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantTrimethylsilylacetyleneHCID 66111—
Reactantmethyl N-(5-bromo-2-fluorobenzyl)carbamateHCID 15483912—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventTriethylamineHCID 8471—
Productmethyl N-[2-fluoro-5-(trimethylsilylethynyl)benzyl]carbamateHCID 1548391583.1%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture comprising 8.00 g of methyl N-(5-bromo-2-fluorobenzyl)carbamate, 4.50 g of trimethylsilylacetylene, 0.96 g of dichlorobis(triphenylphosphine)palladium, 0.47 g of copper(I) iodide and 30 ml of triethylamine, was stirred at 90° C. for 48 hours in an autoclave. This reaction solution was poured into a saturated sodium chloride aqueous solution and extracted with ethyl acetate, followed by drying over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography to obtain 7.09 g of methyl N-[2-fluoro-5-(trimethylsilylethynyl)benzyl]carbamate as a brown viscous liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313071B1
Source datasetuspto-grants-2001_11
ORD IDord-4f0057aa1bf448a9834ea4385fc23e77
Source noteuspto-grants-2001_11