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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2104290Generated: October 30, 2026

Triethylamine → HCID 18765786, compound

https://huagongshe.com/reaction/2104290

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant5-Methoxysalicylic AcidHCID 75787—
ReactantBenzeneethanamine, 4-nitro-, hydrochloride (1:1)HCID 458983—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 178418300HCID 178418300—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 18765786HCID 1876578664%

Reaction Conditions

Temperature25 °C

Reaction Steps

4-nitrophenethylamine hydrochloride (1.81 g; 8.9 mmol), triethylamine (2.8 ml; 20 mmol), hydroxybenzotriazole (1.45 g; 10.7 mmol) and 1-(3-dimethylaminopropyl)-3-ethyl-carbodiimide hydrochloride (3.75 g; 19.62 mmol) are added to a solution of 1.5 g (8.9 mmol) of 5-methoxy-salicylic acid in dichloromethane (80 ml). The reaction medium is agitated overnight at 25° C. The mixture is diluted with 40 ml of water and agitated for ten minutes, then the product is extracted with dichloromethane. The organic solution is dried over sodium sulphate, filtered and concentrated under vacuum and the evaporation residue is purified on a silica column (eluent=ethyl acetate/heptane; 50/50) in order to produce a white solid which is obtained with a yield of 64%. Melting point: 200° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576241B2
Source datasetuspto-grants-2009_08
ORD IDord-cd9741f0d903414a81ebc14913e59441
Source noteuspto-grants-2009_08