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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1178878Generated: October 26, 2026

Formaldehyde → N-tert-Butyl-N-(methoxymethyl)-N-(trimethylsilylmethyl)amine

https://huagongshe.com/reaction/1178878

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantMethanolHCID 887—
ReactantPotassium CarbonateHCID 11430—
ReactantN-tert-Butyl-N-(trimethylsilylmethyl)amineHCID 425246—
SolventWaterHCID 962—
ProductN-tert-Butyl-N-(methoxymethyl)-N-(trimethylsilylmethyl)amineHCID 22228418—

Reaction Steps

N-tert-Butyl-N-(trimethylsilylmethyl)amine from Step A (8.47 g, 53.1 mmol) was added dropwise, over approximately 30 minutes, via a pressure equalizing addition funnel to a stirred solution of aqueous formaldehyde (5.98 mL of a 37 wt. % solution in water, 79.7 mmol) at 0° C. (ice cooling). After 45 minutes, methanol (6.45 mL, 159.3 mmol) was added and the resulting solution was saturated with potassium carbonate. After stirring vigorously for approximately 5 h, the aqueous phase was removed. The organic phase was saturated with potassium carbonate and stirred overnight. The reaction mixture was poured into water and extracted three times with diethyl ether. The combined organic extracts were washed with brine, dried (MgSO4) and the volatiles evaporated in vacuo. Distillation (high vacuum; ˜70° C.) of the residual liquid afforded the title compound as a colorless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07276520B2
Source datasetuspto-grants-2007_10
ORD IDord-e338a028fbc14ba2aaed2d5ae3d31166
Source noteuspto-grants-2007_10