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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1854632Generated: October 25, 2026

N-Allyl-1,1,1-trimethyl-N-(trimethylsilyl)silylamine → 1,5-dimethyl-5-(N,N-bistrimethylsilylaminopropyl)-1-aza-4,6-dioxa-5-silacyclooctane

https://huagongshe.com/reaction/1854632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Allyl-1,1,1-trimethyl-N-(trimethylsilyl)silylamineHCID 82125—
Reactant1,5-Dimethyl-1-aza-4,6-dioxa-5-silacyclooctaneHCID 123163200—
CatalystPlatinumHCID 23939—
Product1,5-dimethyl-5-(N,N-bistrimethylsilylaminopropyl)-1-aza-4,6-dioxa-5-silacyclooctaneHCID 6797990411.9%

Reaction Conditions

Temperature75 °C

Reaction Steps

To a sealed 300 mL nitrogen purged glass bottle was added 16.2 g (100 mmol) 1,5-dimethyl-1-aza-4,6-dioxa-5-silacyclooctane and 20.1 g (100 mmol) N,N-bistrimethylsilylallylamine and the bottle was heated to 75° C. with stirring. Then, 0.8 mL of a 2 wt % platinum solution of Karsted's catalyst in xylenes was added to the reaction. After 24 hrs, the product was isolated by vacuum distillation at 110° C. and 0.04 mm Hg (4.33 g, 11.9% yield). 1H NMR (300 MHz, C6D6) δ (ppm) 3.72 (4H, t), 2.71 (2H, t), 2.59 (4H, t), 2.41 (3H, s), 1.44-1.42 (2H, m), 0.44 (2H, t), 0.09 (3H, s), 0.06 (18H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962745B2
Source datasetuspto-grants-2015_02
ORD IDord-573cfd0ae37b4d0185c6d9a967cea445
Source noteuspto-grants-2015_02