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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 589227Generated: October 26, 2026

Hydrochloric Acid → Bis{3-(triallylsilyl)propyl}(methoxy)methylsilane

https://huagongshe.com/reaction/589227

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl EtherHCID 3283—
ReactantTrimethoxymethyl silaneHCID 101924291—
ReactantHCID 178460902HCID 178460902—
SolventWaterHCID 962—
ProductBis{3-(triallylsilyl)propyl}(methoxy)methylsilaneHCID 13173446062%

Reaction Conditions

Temperature0 °C

Reaction Steps

Under a nitrogen atmosphere, trimethoxymethylsilane (18) (42 μl, 0.3 mmol) was added into a reaction container, cooled down to 0° C. and then diethyl ether solution of 0.9M 3-(triallylsilyl)propylmagnesium bromide (24) (1 mL, 0.9 mmol) was dropped. After dropping, stirring was continued at room temperature for 5 hours. To the reacted mixture, water was added to stop the reaction, then 10% hydrochloric acid was added until the salt was completely dissolved. The obtained organic layer was separated and the obtained water layer was extracted with diethyl ether. The collected organic layer was washed each with saturated sodium bicarbonate aqueous solution and saturated saline solution in this order, then dried over anhydrous magnesium sulfate, filtered, concentrated under reduced pressure, obtaining bis{3-(triallylsilyl)propyl}(methoxy)methylsilane (35) represented by the following chemical reaction equation (yield: 85 mg, yield (%): 62%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09228107B2
Source datasetuspto-grants-2016_01
ORD IDord-7880462910c048e7bddbc15f0f4a2f52
Source noteuspto-grants-2016_01