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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1691797Generated: October 25, 2026

4-Methoxypyridine → 4-Methoxy-3-(triisopropylsilyl)pyridine

https://huagongshe.com/reaction/1691797

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethoxypyridineHCID 69278—
ReactantTriisopropylsilyl chlorideHCID 139400—
ReactantLithium diisopropylamideHCID 2724682—
ReactantTetrahydrofuran heptane ethylbenzolHCID 22742125—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4-Methoxy-3-(triisopropylsilyl)pyridineHCID 1090152422.2%

Reaction Conditions

Temperature-25 °C

Reaction Steps

Following the procedure reported in JACS 1994, 116, 4719-4728, to a solution of 4-methoxypyridine (14.0 g, 128.3 mmol) in THF (150 mL) was added at −25° C., 2.0M LDA in heptane/THF/ethyl benzene (76.9 mL, 153.9 mmol). The mixture was stirred at −25° C. for 30 minutes. Triisopropylsilyl chloride (35.3 mL, 166.8 mmol) was added and the mixture was stirred at −25° C. for 15 minutes and then at room temperature for 16 hours. Water was added and the mixture was extracted with EtOAc. The extract was washed with water, brine dried over MgSO4 and concentrated to dryness. Purification of the residue by flash chromatography (hexane/ethylacetate 8:2-1:1) gave 4-methoxy-3-triisopropylsilanyl-pyridine (7.56 g, 22%) as an orange solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153809B2
Source datasetuspto-grants-2012_04
ORD IDord-df314cae4932467eb12a3899b6d43f09
Source noteuspto-grants-2012_04