Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2352073Generated: November 1, 2026

Triethylamine → HCID 86743465, compound

https://huagongshe.com/reaction/2352073

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantVinyltrimethylsilaneHCID 79102—
ReactantTri-o-tolylphosphineHCID 80271—
ReactantHCID 13799217HCID 13799217—
CatalystPalladium ChlorideHCID 24290—
SolventDimethylformamideHCID 6228—
ProductHCID 86743465HCID 86743465—

Reaction Steps

In a small autoclave, 1.15 g of 1,1-diethyl-3-(2-iodo-1-propyl-6-methyl-8α-ergolinyl)urea is heated under argon for 3 hours to a bath temperature of 115° C. in 10 ml of dimethylformamide with 10 ml of triethylamine, 53.5 mg of triorthotolylphosphine, 39.4 mg of palladium(II) chloride and 1.34 ml of vinyltrimethylsilane. After evaporation, the mixture is distributed in methylene chloride/sodium bicarbonate solution. The organic phase is evaporated and chromatographed over silica gel with ethyl acetate: ethanol=3:1 as the eluent, thus obtaining 218 mg of 1,1-diethyl-3-(2-trimethylsilylvinyl-1-propyl-6-methyl-8α-ergolinyl)urea and 230 mg of 1,1-diethy-3-(2-vinyl-1-propyl-6-methyl-8α-ergolinyl)urea as oils.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04874768
Source datasetuspto-grants-1989_10
ORD IDord-d7e8b27d4cf54f86bf28f6b2818d0e4e
Source noteuspto-grants-1989_10