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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 279214Generated: October 31, 2026

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

https://huagongshe.com/reaction/279214

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllylamineHCID 7853—
ReactantSodium HydroxideHCID 14798—
ReactantSilane, (chloromethyl)trimethyl-HCID 75361—
SolventWaterHCID 962—
ProductN-((trimethylsilyl)methyl)prop-2-en-1-amineHCID 1248958772.7%

Reaction Conditions

Temperature70 °C

Reaction Steps

To 118 mL (1.57 mol) of allylamine warmed at 40° C. in an inert atmosphere was very slowly added 100 mL (0.72 mol) of chloromethyl trimethylsilane (approximate rate of 1 mL/min). The reaction mixture was slowly warmed to 70° C. and stirred for 24 h. The reaction mixture was cooled to 0° C. and to it was added water to break up the gel and then 300 mL of 2N NaOH solution. The reaction mixture was extracted with ether. The combined organic fractions were washed with 500 mL of sat'd NaCl solution, dried over Na2SO4, filtered and the filtrate was concentrated. The residue was purified by distillation (bp 80-84° C. @ 100 torr) to give 75 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06362201B1
Source datasetuspto-grants-2002_03
ORD IDord-3f22cc22fc3945dabe3dbc31a0321663
Source noteuspto-grants-2002_03