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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2425527Generated: October 30, 2026

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

https://huagongshe.com/reaction/2425527

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantMethanolHCID 887—
ReactantPotassium CarbonateHCID 11430—
ReactantN-((trimethylsilyl)methyl)prop-2-en-1-amineHCID 12489587—
SolventWaterHCID 962—
Solventtert-Butyl methyl etherHCID 15413—
ProductN-(methoxymethyl)-N-((trimethylsilyl)methyl)prop-2-en-1-amineHCID 1837474287.4%

Reaction Steps

To N-((trimethylsilyl)methyl)prop-2-en-1-amine (21 g, 146.5 mmol) was slowly added aqueous formaldehyde (20 g; 37% w/w) while stirring at room temperature. After 5 minutes additional stirring methanol (8 g) was added followed by the addition of K2CO3 (24 g). The reaction mixture was stirred overnight at room temperature. Water (100 ml) was added, followed by addition of tert-butyl methyl ether (75 ml). The organic layer was separated. The aqueous layer was extracted with tert-butyl methyl ether (75 ml). The combined organic extracts were dried with Na2SO4. Concentration under vacuum gave N-(methoxymethyl)-N-((trimethylsilyl)methyl)prop-2-en-1-amine as a clear oil (24 g, 128.1 mmol) in 87% c.y.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07964739B2
Source datasetuspto-grants-2011_06
ORD IDord-2737a701769245c38e20c84ef9225fa2
Source noteuspto-grants-2011_06