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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2187478Generated: October 26, 2026

Triethylamine → Diisopropylether ethyl acetate

https://huagongshe.com/reaction/2187478

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantThionyl ChlorideHCID 24386—
Reactant4-(Morpholine-4-carbonyl)anilineHCID 577815—
Reactant5-Methoxy-8-nitro-1,2,3,4-tetrahydronaphthalene-2-carboxylic acidHCID 18622509—
CatalystDimethylformamideHCID 6228—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
ProductN-(4-Morpholinocarbonylphenyl)-5-methoxy-8-nitro-1,2,3,4-tetrahydronaphthalene-2-carboxamideHCID 18622500—
ProductDiisopropylether ethyl acetateHCID 22281796315.3%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 5-methoxy-8-nitro-1,2,3,4-tetrahydronaphthalene-2-carboxylic acid (1.0 g, 4 mmol), toluene (20 mL), N,N-dimethylformamide (10 drops) and thionyl chloride (1.5 mL, 20 mmol) was heated at 60° C. for 1 h. The solvents were removed in vacuo and the residue, dissolved in methylene chloride (20 mL), was added to a solution of 4-aminobenzoylmorpholine (820 mg, 4 mmol, described in: Devlin J.P. J. Chem. Soc. Perkin Trans I, 1975, 830-841) and triethylamine (800 mg, 8 mmol) in methylene chloride (30 mL) at 5° C. After stirring at 20° C. for 2 h, water was added and the organic phase was separated, dried and the solvent removed in vacuo. The oily residue was crystallized from diisopropyl ether/ethyl acetate affording 1.2 g (73% yield) of the title compound as crystals: mp 186-189° C.; EIMS (70 eV) m/z (relative intensity) 439 (20, M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06410532B1
Source datasetuspto-grants-2002_06
ORD IDord-dc87a79c201c47a690d0746e989a239e
Source noteuspto-grants-2002_06