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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 520414Generated: October 25, 2026

Diisopropylamine → Tert-butyl((1,2-dimethoxyprop-1-en-1-yl)oxy)dimethylsilane

https://huagongshe.com/reaction/520414

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantPropanoic acid, 2-methoxy-, methyl esterHCID 86599—
ReactantLithium diisopropylamideHCID 2724682—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl((1,2-dimethoxyprop-1-en-1-yl)oxy)dimethylsilaneHCID 86130319—

Reaction Conditions

Temperature-20 °C

Reaction Steps

A solution of methyl 2-methoxypropionate (177 mg, 1.5 mmol) in THF (1 mL) was added to a solution of LDA prepared from diisopropylamine (0.212 mL, 1.50 mmol) and butyllithium (0.60 mL, 1.50 mmol) in THF (2 mL) at −78° C. under nitrogen. The mixture was gradually allowed to warm to −20° C. over 1 h, re-cooled to −78° C. and then a solution of tert-butylchlorodimethylsilane (233 mg, 1.50 mmol) in THF (1 mL) was added. The mixture was allowed to warm to rt over 2 h and stirred overnight. The reaction was quenched with satd. NaHCO3 (5 mL), diluted with DCM (10 mL). The organic layer was separated, washed with water, brine and dried (MgSO4). Evaporation of solvents afforded tert-butyl((1,2-dimethoxyprop-1-en-1-yl)oxy)dimethylsilane as a clear oil and used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09326973B2
Source datasetuspto-grants-2016_05
ORD IDord-842df4223b95441b84cabe8d66a92937
Source noteuspto-grants-2016_05