Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 649253Generated: October 29, 2026

Triethylamine → HCID 54082176, compound

https://huagongshe.com/reaction/649253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantChlorodimethylphenylsilaneHCID 13029—
ReactantCrotonaldehydeHCID 447466—
CatalystZincchlorideHCID 3007855—
SolventTolueneHCID 1140—
ProductHCID 54082176HCID 5408217659%

Reaction Steps

A 250 mL flask, fitted with a magnetic stirrer, a reflux condenser and an addition funnel, was charged with zinc chloride (0.25 g, 1.83 mmol, anhydrous), triethylamine (36.2 mL, 0.260M, distilled from CaH2), crotonaldehyde (21.0 mL, 0.257M, dried over MgSO4 and distilled), and toluene (35 mL, distilled from sodium). 42 mL of phenyldimethyl chlorosilane (0.254M) were added dropwise via the addition funnel over one hour with stirring. The resulting mixture was heated slowly to about 65° and maintained at 65°-75° for a total of 6.5 hours with stirring. The mixture was cooled to ambient temperature and filtered to remove precipitated triethylamine hydrochloride (32 g, 92%) which was rinsed on the filter with 35 mL of dry toluene. The resulting filtrate and rinse were combined and distilled on a water pump at about 110 mm to remove solvent and unreacted starting materials. The resulting residue was distilled on an oil pump to give (1,3-butadienyloxy)phenyldimethylsilane (30.9 g, 59%) as a colorless liquid boiling at 57.8°-59.0°/0.10 mm (13 Pa).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04739021
Source datasetuspto-grants-1988_04
ORD IDord-c2a5ed2404c04a50aafa379b3d13b961
Source noteuspto-grants-1988_04