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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1760584Generated: November 3, 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/1760584

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 68890098—

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 4:1 hexane:ethyl acetateto yield 1.92 g of the title compound as a light brown oil. MS: M+NH4+=457.0 M+Na+=462.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06844345B2
Source datasetuspto-grants-2005_01
ORD IDord-f8ab1de3937a4bbf88b38e5b6cbc4a05
Source noteuspto-grants-2005_01