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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2351650Generated: November 1, 2026

1,1-bis(1,1-dimethylethoxy)-N,N,N-trimethylamine → HCID 14390471, compound

https://huagongshe.com/reaction/2351650

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1-bis(1,1-dimethylethoxy)-N,N,N-trimethylamineHCID 547712—
ReactantHCID 15617180HCID 15617180—
SolventBenzeneHCID 241—
ProductHCID 14390471HCID 1439047145.1%

Reaction Steps

Under a nitrogen atmosphere, N,N-dimethylformamide-ditert-butyl acetal (8.12 g, 0.040 mole) was added dropwise over a 20-minute period to a stirred, refluxing suspension of 2-(2-pyridyl)-3H-imidazo[4,5-b]pyridine-3-acetic acid (2.54 g, 0.010 mole) in anhydrous benzene (50 ml). The resulting solution was refluxed for 1 hour and allowed to cool to room temperature. The reaction mixture was washed with 10% potassium carbonate solution (2×25 ml), water (25 ml), dried over sodium sulfate and concentrated in vacuo. The residue (3.5 g) was dissolved in tetrahydrofuran and treated with excess ethereal hydrogen chloride. The crystalline solid was recrystallized from tetrahydrofuran, giving 1.5 g (43%). Drying in vacuo at 65° C. for 8 hours and then at 78° C. overnight gave 1.4 g of the compound as the free base, mp 124°-125.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04873251
Source datasetuspto-grants-1989_10
ORD IDord-171c3beb4f5a4c818711972ac503fd07
Source noteuspto-grants-1989_10