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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2425526Generated: November 4, 2026

Allylamine → N-((trimethylsilyl)methyl)prop-2-en-1-amine

https://huagongshe.com/reaction/2425526

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllylamineHCID 7853—
ReactantSodium HydroxideHCID 14798—
ReactantSilane, (chloromethyl)trimethyl-HCID 75361—
SolventWaterHCID 962—
ProductN-((trimethylsilyl)methyl)prop-2-en-1-amineHCID 1248958781.4%

Reaction Conditions

Temperature70 °C

Reaction Steps

Allylamine (29.5 ml, 392.5 mmol) was warmed to 40° C. under nitrogen atmosphere. Chloromethyltrimethylsilane (25.0 ml, 180 mmol) was added very slowly to the allylamine while stirring. After the addition was complete the mixture was warmed to 70° C. for 24 hours. The mixture was cooled to 0° C. and water (25 ml) was added, followed by 2 N NaOH solution (75 ml). The mixture was stirred for one hour and was then extracted with tert-butyl methyl ether (tBME; 2×100 ml). The organic layer was dried with Na2SO4 and then concentrated under vacuum at 300 mbar at 70° C. to give pure N-((trimethylsilyl)methyl)prop-2-en-1-amine (21 g, 146.5 mmol) in 81% c.y.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07964739B2
Source datasetuspto-grants-2011_06
ORD IDord-a2a3022960dc45328e3304b28f3dc2ac
Source noteuspto-grants-2011_06