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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754961Generated: October 28, 2026

Water → (4-Bromo-5-methyl-2-trimethylsilanylethynyl-phenyl)-carbamic acid methyl ester

https://huagongshe.com/reaction/1754961

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantMethyl (4-Bromo-2-iodo-5-methylphenyl)carbamateHCID 57543475—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418476HCID 178418476—
SolventTetrahydrofuranHCID 8028—
Product(4-Bromo-5-methyl-2-trimethylsilanylethynyl-phenyl)-carbamic acid methyl esterHCID 6681622498.2%

Reaction Steps

(4-Bromo-2-iodo-5-methyl-phenyl)-carbamic acid methyl ester (605 mg, 1.64 mmol) was dissolved in THF (6 ml). (Trimethylsilyl)acetylene (0.70 ml, 4.95 mmol), copper iodide (33.5 mg, 0.175 mmol), Pd(PPh3)2Cl2 (56.5 mg, 0.081 mmol) and triethylamine (0.690 ml, 4.95 mmol) were added and the mixture was stirred at room temperature for four hours. Water was added to the reaction system, followed by extraction with ethyl acetate. The organic layer was washed with water and saturated brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (n-hexane-ethyl acetate) to give (4-bromo-5-methyl-2-trimethylsilanylethynyl-phenyl)-carbamic acid methyl ester (548 mg, 98%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169254B2
Source datasetuspto-grants-2015_10
ORD IDord-771d5be57ea242c48f04c7a35d2f0c28
Source noteuspto-grants-2015_10