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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-tert-Butyl-N-(trimethylsilylmethyl)amine | HCID 425246 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-tert-Butyl-N-(methoxymethyl)-N-(trimethylsilylmethyl)amine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07276520B2 |
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| Source dataset | uspto-grants-2007_10 |
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| ORD ID | ord-e338a028fbc14ba2aaed2d5ae3d31166 |
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| Source note | uspto-grants-2007_10 |
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