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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 853096Generated: October 29, 2026

Dimethyl (2-propynyloxy)(1,1,2-trimethylpropyl)-silane → (4-Bromo-2-{3-[dimethyl-(1,1,2-trimethyl-propyl)-silanyloxy]-prop-1-ynyl}-5-methyl-phenyl)-carbamic acid methyl ester

https://huagongshe.com/reaction/853096

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl (2-propynyloxy)(1,1,2-trimethylpropyl)-silaneHCID 18455989—
ReactantMethyl (4-Bromo-2-iodo-5-methylphenyl)carbamateHCID 57543475—
SolventTriethylamineHCID 8471—
Product(4-Bromo-2-{3-[dimethyl-(1,1,2-trimethyl-propyl)-silanyloxy]-prop-1-ynyl}-5-methyl-phenyl)-carbamic acid methyl esterHCID 6889009843.6%

Reaction Steps

To a solution of 3.70 g (4-bromo-2-iodo-5-methyl-phenyl)-carbamic acid methyl ester and 0.070 g bis-triphenylphosphine palladium dichloride and 0.038 g cuprous iodide in 25 ml triethylamine was added 2.38 g dimethyl (2-propynyloxy)(1,1,2-trimethylpropyl)-silane and the mixture was heated 2 h at reflux. The reaction mixture was partitioned between water and ethyl acetate. The phases were separated and the organic phase was washed with 1N hydrochloric acid, sodium bicarbonate and brine, dried with magnesium sulfate and purified by chromatography on silica gel with hexane:ethyl acetate=4:1 to yield 1.92 g (4-bromo-2-{3-[dimethyl-(1,1,2-trimethyl-propyl)-silanyloxy]-prop-1-ynyl}-5-methyl-phenyl)-carbamic acid methyl ester as a light brown oil. MS: M+NH4+=457.0 M+Na+=462.2

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253281B2
Source datasetuspto-grants-2007_08
ORD IDord-3822e9602b8a4b2c88b8a9bcde58ab84
Source noteuspto-grants-2007_08