HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2382227Generated: October 25, 2026
N-Allyl-1,1,1-trimethyl-N-(trimethylsilyl)silylamine → N-trimethylsilyl-2-chloro-2-methy-1-aza-2-silacyclopentane
https://huagongshe.com/reaction/2382227
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-Allyl-1,1,1-trimethyl-N-(trimethylsilyl)silylamine | HCID 82125 | — |
| Reactant | (Dichloromethyl)silane | HCID 57353436 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | N-trimethylsilyl-2-chloro-2-methy-1-aza-2-silacyclopentane | HCID 67301002 | — |
Reaction Steps
N-trimethylsilyl-2-chloro-2-methy-1-aza-2-silacyclopentane (cyclic APMCS, which may be referred to as c-APMCS) was prepared as follows. To a 300 mL nitrogen purged bottle equipped with stir bar was added 20.1 g (0.1 mol) of N,N-bis(trimethylsilyl)allyl amine, 11.5 g (0.1 mol) of dichloromethylsilane, and 0.81 mL of 2.4 wt % Karsted's Catalyst in xylene. The solution was stirred for 72 hrs, then heated at 65° C. for 2 hrs, and heated at 100° C. for a further 3 days. The product was distilled at 85-90° C. at 25 mm Hg. GC/MS confirmed structure. Proton NMR was also used to determine structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08258332B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-7b068095cd93427aadd57b2c0f15b16d |
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| Source note | uspto-grants-2012_09 |
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