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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033754Generated: October 26, 2026

Triethylamine → HCID 15232643, compound

https://huagongshe.com/reaction/1033754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-OctanolHCID 20083—
Reactant2-DimethylaminopyridineHCID 21885—
Reactant2,3,5-Triiodobenzoyl chlorideHCID 2760806—
SolventDichloromethaneHCID 6344—
ProductHCID 15232643HCID 15232643—

Reaction Conditions

Temperature0 °C

Reaction Steps

The 2,3,5-triiodobenzoyl chloride was dissolved in 60 ml of dry dichloromethane. The solution was cooled to 0° C. and 6.07 g (60.0 mmol) of triethylamine was added. The brown solution was placed under nitrogen and 4.30 g (33.0 mmol) of 2-octanol was added in 10 ml of dry dichloromethane. Dimethylaminopyridine (0.367 g, 3.00 mmol) was added and the resulting solution was stirred at room temperature for 72 hrs. The brown solution was partitioned between 100 ml of dichloromethane and 100 ml of 1M HCl. The dichloromethane layer was washed with saturated NaHCO3 solution (50 ml) and brine (50 ml). The solution was dried over Na2SO4 and concentrated in vacuo to yield a dark brown oil (17.43 g). The oil was purified by flash chromatography using 436 g of silica gel and 5% ethyl acetate/hexane as the eluent. The first 600 ml to elute contained nothing while the pure product eluted with the next 700 ml. Concentration in vacuo afforded 15.68 g (85%) of the product as a yellow tinted oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05312616
Source datasetuspto-grants-1994_05
ORD IDord-d92ec52fb91c493a8f3bafb083ae5d90
Source noteuspto-grants-1994_05