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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1955497Generated: November 2, 2026

Vinyltrimethoxysilane → HCID 19070353, compound

https://huagongshe.com/reaction/1955497

Reaction equation

Participants

RoleNameHCIDCharge
ReactantVinyltrimethoxysilaneHCID 76004—
Reactant2-Benzyl-2-(dimethylamino)-1-(4-(morpholin-4-yl)phenyl)butan-1-oneHCID 86171—
SolventTolueneHCID 1140—
ProductHCID 19070353HCID 1907035367%

Reaction Steps

14.6 g (40 mmol) of 2-benzyl-2-dimethylamino-1-(4-morpholinophenyl)-1-butanone, 750 mg (0.8 mmol) of RuH2 (CO) (PPh3)3 and 13.4 ml (88 mmol) of vinyltrimethoxysilane were dissolved in 50 ml of toluene and degased using N2. After heating with stirring at reflux for 41 hours, the solvent was distilled off and the product was chromatographed (silica gel, CH2Cl2 /ethyl acetate). 13.8 g (67%) of dark red oil were obtained which were purified by boiling in heptane with active charcoal followed by filtration to give a yellow, viscous oil. 1H-NMR (CDCl3): 0.61 ppm (3H, t, Bu-H4, 3JH,H =7.2 Hz); 1.2 ppm (2H, mc, Et-H2); 1.88 ppm (2H, mc, Bu-H3); 2.37 ppm (6H, s, N(CH3)2); 2.71 ppm (2H, mc, Et-H1); 3.16 ppm (2H, mc, CH2 -Ph); 3.25 ppm (4H, mc, morpholine-N--CH2); 3.63 ppm (9H, s, Si(OCH3)3); 3.85 ppm (4H), mc, morpholine-O-CH2); 6.61 ppm (1H, dd, Ph-H5, 3JH5,H6, =8.6 Hz, 4 JH3, H6 =2.6 Hz); 6.75 ppm (1H, d, Ph-H3); 7.14-7.29 ppm (5H, m, Ph'-H); 8.44 ppm (1H, d, Ph-H6).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05776658
Source datasetuspto-grants-1998_07
ORD IDord-db06e0d327474187bdbb0d431c2a3536
Source noteuspto-grants-1998_07