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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1398119Generated: November 1, 2026

Hydrazine hydrate (1:1) → 3-Methoxy-4-(2-methyloxazol-5-yl)benzohydrazide

https://huagongshe.com/reaction/1398119

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant3-Methoxy-4-(2-methyl-1,3-oxazol-5-yl)benzoic acidHCID 66607777—
SolventTetrahydrofuranHCID 8028—
Product3-Methoxy-4-(2-methyloxazol-5-yl)benzohydrazideHCID 66607961—

Reaction Conditions

Temperature-10 °C

Reaction Steps

N,N′-Carbonyldiimidazole (115 g) was added to a suspension of 3-methoxy-4-(2-methyl-1,3-oxazol-5-yl)benzoic acid (83.0 g) in THF (1 L) at room temperature, and the mixture was stirred for 1 hr. The reaction mixture was cooled to −10° C., hydrazine monohydrate (173 mL) was added, and the mixture was stirred at room temperature for 16 hr. The solvent in the reaction mixture was evaporated under reduced pressure, and water was added to the residue. The resultant solid was collected by filtration, washed with water, dried under reduced pressure, and washed with IPE to give the title compound (85.8 g). 1H NMR (300 MHz, DMSO-d6) δ 2.48 (3H, s), 3.97 (3H, s), 4.53 (2H, brs), 7.44-7.58 (3H, m), 7.68 (1H, d, J=8.0 Hz), 9.85 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901309B2
Source datasetuspto-grants-2014_12
ORD IDord-1bf489e4695647f4ac9b6ec6aaa49875
Source noteuspto-grants-2014_12