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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 600481Generated: October 28, 2026

N,N,N',N'-Tetramethylazodicarboxamide → HCID 42635829, compound

https://huagongshe.com/reaction/600481

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N,N',N'-TetramethylazodicarboxamideHCID 4278—
ReactantTriphenylphosphineHCID 11776—
ReactantTributylphosphineHCID 13831—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant(5-Methyl-3-phenyl-1,2-oxazol-4-yl)methanolHCID 2776149—
ReactantHCID 178516710HCID 178516710—
SolventTetrahydrofuranHCID 8028—
ProductHCID 42635829HCID 4263582940%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of (5-methyl-3-phenyl-isoxazol-4-yl)-methanol (100 mg, 0.53 mmol) in THF (6 mL) was added 2-hydroxyquinoxaline (77 mg, 0.53 mmol) and tributyl phosphine (206 μL, 0.79 mmol) at ambient temperature under an argon atmosphere. After cooling to 0° C., N,N,N′,N′-tetramethylazodicarboxamide (137 mg, 0.79 mmol) was added. The resulting orange solution was stirred for 16 h at ambient temperature followed by 2.5 h at 50° C. Then triphenylphosphine (208 mg, 0.79 mmol), 2-hydroxyquinoxaline (77 mg, 0.53 mmol) and diethyl azodicarboxylate (127 μL, 0.79 mmol) were added and the reaction mixture was stirred for 4 h at 50° C. The reaction mixture was then evaporated. Purification by chromatography (SiO2, heptane:ethyl acetate=95:5 to 0:100) afforded the title compound (67 mg, 40%) as a white solid. MS: m/e=318.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902201B2
Source datasetuspto-grants-2011_03
ORD IDord-f0b535d1f41f4280bf4725876242190f
Source noteuspto-grants-2011_03