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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10563Generated: October 26, 2026

N,N,N',N'-Tetramethylazodicarboxamide → HCID 178418876, compound

https://huagongshe.com/reaction/10563

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N,N',N'-TetramethylazodicarboxamideHCID 4278—
Reactant4-Methoxybenzoic AcidHCID 7478—
ReactantTributylphosphineHCID 13831—
ReactantHCID 178418329HCID 178418329—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 178418876HCID 17841887696.3%

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of Intermediate 35 (21.06 g), 1,1′-azobis(N,N-dimethylformamide) (64.11 g) and p-anisic acid (23.03 g, Tokyo Kasei Kogyo) in tetrahydrofuran (400 ml) was added with tri(n-butyl)phosphine (35.6 ml) at room temperature and stirred at 50° C. for 2.5 hours. The reaction mixture was cooled to room temperature, then added with ethyl acetate (200 ml) and successively washed with saturated aqueous sodium hydrogencarbonate twice (200 ml each) and 0.1 N aqueous sodium hydroxide (50 ml), and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=5:1) to obtain the title compound (32.92 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07094789B2
Source datasetuspto-grants-2006_08
ORD IDord-6de56dfb6df84ba996ea22062f1fd467
Source noteuspto-grants-2006_08