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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1043474Generated: October 26, 2026

2,6-Lutidine → [(3,5-Dichlorobenzyl)oxy](triisopropyl)silane

https://huagongshe.com/reaction/1043474

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-LutidineHCID 7937—
Reactant3,5-Dichlorobenzylic alcoholHCID 43236—
ReactantTriisopropylsilyl trifluoromethanesulfonateHCID 2724529—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product[(3,5-Dichlorobenzyl)oxy](triisopropyl)silaneHCID 1173909679%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of (3,5-dichlorophenyl)methanol (10.0 g, 56.5 mmol) in methylene chloride (100 mL) at 0° C. was added 2,6-lutidine (16.4 mL, 141 mmol) followed by triisopropylsilyl triflate (19.7 mL, 73.4 mmol), and was stirred at 0° C. for 2 hours. The reaction was diluted with water and the organic layer was separated, washed with brine, dried over Na2SO4, filtered and concentrated. The residue was purified by chromatography on silica gel, eluting with hexane to provide the desired product (14.8 g, 79%). LC/MS: 333 (M+H)+, 1H NMR (CDCl3) δ 7.23 (s, 3H), 4.78 (s, 2H), 1.18 (m, 3H), 1.03 (s, 18H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563541B2
Source datasetuspto-grants-2013_10
ORD IDord-9c302fb4ab2c41969397f669fa46f4f0
Source noteuspto-grants-2013_10