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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 613599Generated: October 31, 2026

Hydrazine hydrate (1:1) → 2-amino-3-benzyloxy-N-methylaniline

https://huagongshe.com/reaction/613599

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant3-benzyloxy-2-nitro-N-methylanilineHCID 10729890—
SolventMethanolHCID 887—
Product2-amino-3-benzyloxy-N-methylanilineHCID 1048954187.1%

Reaction Steps

To a mixture of 3-benzyloxy-N-methyl-2-nitroaniline (453.3 mg), 80% methanol (6.8 ml), anhydrous ferric chloride (13.6 mg) and carbon (13.6 mg) was dropwise added hydrazine monohydrate (255.6 μl) at 70° C., and the mixture was stirred for 5 hours at the same temperature. Insoluble material was filtered off, and the filtrate was concentrated in vacuo. Ethyl acetate and saturated sodium bicarbonate solution were added to the residue, and the organic layer was washed with water and brine, dried over magnesium sulfate and concentrated in vacuo. The residue was purified by column chromatography on silica gel (ethyl acetate-n-hexane) to give 2-amino-3-benzyloxy-N-methylaniline (348.9 mg). mp: 79-81° C., NMR (CDCl3, δ): 2.87 (3H, s), 3.43 (3H, br s), 5.07 (2H, s), 6.40 (1H, d, J=7.5 Hz), 6.49 (1H, d, J=7.5 Hz), 6.80 (1H, t, J=7.5 Hz), 7.29-7.47 (5H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06008229
Source datasetuspto-grants-1999_12
ORD IDord-89e3579cf22a4c9680c702153096afa2
Source noteuspto-grants-1999_12