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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518597Generated: October 25, 2026

2,6-Lutidine → (3-Fluoro-4-nitrobenzyloxy)triisopropylsilane

https://huagongshe.com/reaction/518597

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-LutidineHCID 7937—
ReactantTriisopropylsilyl trifluoromethanesulfonateHCID 2724529—
Reactant3-Fluoro-4-nitrobenzyl alcoholHCID 2774658—
SolventDichloromethaneHCID 6344—
Product(3-Fluoro-4-nitrobenzyloxy)triisopropylsilaneHCID 6019538499%

Reaction Steps

To a 3-L round-bottomed flask was added (3-fluoro-4-nitrophenyl)methanol (4.7 g, 27.5 mmol) and DCM (47 mL). To the mixture was added triisopropylsilyl trifluoromethanesulfonate (9.26 g, 30.2 mmol) and 2,6-dimethylpyridine (3.53 g, 33.0 mmol). The resulting mixture was stirred for 3 hours at RT, and washed with NH4Cl (5-250 mL) and H2O (5-250 mL). The organic layer was collected and dried over sodium sulfate and concentrated to afford (3-fluoro-4-nitrobenzyloxy)triisopropylsilane (8.9 g, 99% yield) as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115127B2
Source datasetuspto-grants-2015_08
ORD IDord-78eca634cba14ca0a10bcf6f69fde987
Source noteuspto-grants-2015_08