HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1508310Generated: October 30, 2026
Formaldehyde → Benzyl(methoxymethyl)((trimethylsilyl)methyl)amine
https://huagongshe.com/reaction/1508310
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-[(Trimethylsilyl)methyl]benzylamine | HCID 353458 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Benzyl(methoxymethyl)((trimethylsilyl)methyl)amine | HCID 353442 | 75.2% |
Reaction Steps
To a stirred solution of benzyl-trimethylsilanylmethyl-amine (Preparation 28, 25 g, 128.86 mmol) in methanol (300 mL), formaldehyde solution (37-41% w/v, 4.253 g, 141.75 mmol) was added at 0° C. Resulting reaction mixture was stirred at 0° C. for 1 hour and 10-15° C. for 3 hours. K2CO3 (21.34 g, 154.69 mmol) was added to reaction mixture and reaction was stirred at 10-15° C. for 2 hours. After complete consumption of starting material, the resulting reaction mixture was filtered through Buchner funnel; solid was washed by ethyl acetate (3×20 mL). Combined filtrate was concentrated in vacuo to afford product as faint yellow oil (23 g, Crude). Crude compound was used as such for next reaction. (m/z): 195.1 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09221835B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-7317518d491d4643b2e6a9b7aeb442c7 |
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| Source note | uspto-grants-2015_12 |
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