HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2425526Generated: November 4, 2026
Allylamine → N-((trimethylsilyl)methyl)prop-2-en-1-amine
https://huagongshe.com/reaction/2425526
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allylamine | HCID 7853 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Silane, (chloromethyl)trimethyl- | HCID 75361 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-((trimethylsilyl)methyl)prop-2-en-1-amine | HCID 12489587 | 81.4% |
Reaction Steps
Allylamine (29.5 ml, 392.5 mmol) was warmed to 40° C. under nitrogen atmosphere. Chloromethyltrimethylsilane (25.0 ml, 180 mmol) was added very slowly to the allylamine while stirring. After the addition was complete the mixture was warmed to 70° C. for 24 hours. The mixture was cooled to 0° C. and water (25 ml) was added, followed by 2 N NaOH solution (75 ml). The mixture was stirred for one hour and was then extracted with tert-butyl methyl ether (tBME; 2×100 ml). The organic layer was dried with Na2SO4 and then concentrated under vacuum at 300 mbar at 70° C. to give pure N-((trimethylsilyl)methyl)prop-2-en-1-amine (21 g, 146.5 mmol) in 81% c.y.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07964739B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-a2a3022960dc45328e3304b28f3dc2ac |
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| Source note | uspto-grants-2011_06 |
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