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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2209331Generated: October 28, 2026

Triethylamine → HCID 22928264, compound

https://huagongshe.com/reaction/2209331

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthane, 1-chloro-2-ethoxy-HCID 12341—
Reactant2-MethylimidazoleHCID 12749—
ProductHCID 22928264HCID 22928264—

Reaction Steps

In an autoclave of 100 mL, 2-methylimidazole (19.2 g, 200 mmol) was made reacted with chloroethyl ethyl ether (26.0 g, 240 mmol) at 145 deg C. for 72 hours. Brown liquid that was obtained was washed with 120 mL of a compound liquid of ethanol and ether (volume ratio thereof is 1:5), and then made reacted with triethylamine (20.2 g, 200 mmol) in the autoclave of 100 mL at 130 deg C. for 24 hours. Solid salts that was formed was removed by filtration, and residue (filtrate) was subjected to reduced-pressure distillation by using a Vigreux column of 20 cm. The obtained product was a transparent liquid which has a boiling point of 171-175 deg C. when a pressure is 10 Pa. 1H-NMR measurement of obtained amine was performed, and it was confirmed that chemical shifts, δ (ppm), are 6.96 (d, 1H), 6.72(d, 1H), 4.07-4.04(t, 2H), 3.66-3.63 (t, 2H), 3.45-3.40 (m, 2H), 2.29(s, 3H), and 1.12-1.08(t, 3H), and 1-(2-ethoxyethyl)-2-methyl imidazole was synthesized.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09379413B2
Source datasetuspto-grants-2016_06
ORD IDord-ac21cf8337f240dcb5d292465ff91b31
Source noteuspto-grants-2016_06