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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2266781Generated: November 3, 2026

Triethylamine → HCID 24954933, compound

https://huagongshe.com/reaction/2266781

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-ChlorobenzaldehydeHCID 11477—
ReactantBis(2-amino-1H-imidazole) sulphateHCID 135136—
ReactantSodium borohydrideHCID 4311764—
CatalystTitanium isopropoxideHCID 11026—
SolventDichloromethaneHCID 6344—
ProductHCID 24954933HCID 2495493359.9%

Reaction Steps

To a solution of 3-chlorobenzaldehyde (0.16 ml, 1.4 mmol) in dichloromethane (10 ml) were added sequentially 2-aminoimidazole sulfate (0.19 g, 0.7 mmol), tetraisopropyl orthotitanate (0.51 ml, 1.7 mmol) and triethylamine (0.19 ml, 1.4 mmol). The reaction mixture was stirred at room temperature for 16 hours and then concentrated in vacuo. The residue was taken up in ethanol (5 ml) and then sodium borohydride (54 mg, 1.4 mmol) was added. The reaction mixture was stirred at room temperature for 3 hours and then quenched by the addition of water. After stirring for a further 15 minutes at room temperature, the reaction mixture was filtered and the filter cake washed with ethanol. The filtrate was concentrated in vacuo and the residue was purified by chromatography on silica gel (eluant:methanol/dichloromethane 0:100 to 10:90) to yield the title compound as an off-white solid (87 mg, 30%); MS (ISP): 208.7 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858653B2
Source datasetuspto-grants-2010_12
ORD IDord-5a2b9daeae4146c9ac114127c5ca6013
Source noteuspto-grants-2010_12