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HRID 29722作成日:2026年10月27日

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

https://huagongshe.com/reaction/29722

反応式

関与物質

役割名称HCID仕込み量
反応物FormaldehydeHCID 712—
反応物MethanolHCID 887—
反応物Potassium CarbonateHCID 11430—
反応物N-tert-Butyl-N-(trimethylsilylmethyl)amineHCID 425246—
溶媒WaterHCID 962—
生成物N-tert-Butyl-N-(methoxymethyl)-N-(trimethylsilylmethyl)amineHCID 22228418—

反応手順

N-tert-Butyl-N-(trimethylsilylmethyl)amine 77 (8.47 g, 53.1 mmol) was added dropwise, over approximately 30 min, 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. After 45 min, 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 78 as a colorless liquid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07419990B2
出典データセットuspto-grants-2008_09
ORD IDord-4be3b5d08bb7443aa7e8a341d9733152
出典メモuspto-grants-2008_09