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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186641Generated: October 30, 2026

3-Methoxyaniline → HCID 835338, compound

https://huagongshe.com/reaction/1186641

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-MethoxyanilineHCID 10824—
ReactantHCID 779038HCID 779038—
ReactantHCID 819756HCID 819756—
ProductHCID 835338HCID 83533873%

Reaction Steps

N-(3-methoxy-phenyl)-4-nitro-benzenesulfonamide (RK1-1-27D) I This compound was prepared according to the procedure described for compound 11a except using m-anisidine. Recrystallization from DCM/Hexanes obtained the required product as brown-yellow needles (202 mg, 73%). Mp=96-98° C.; 1H NMR (400 MHz, CDCl3) δ 8.29 (d, J=9.0 Hz, 2H), 7.94 (d, J=9.0 Hz, 2H), 7.16 (t, J=8.0 Hz, 1H), 6.73-6.70 (m, 2H), 6.60-6.58 (m, 2H), 3.76 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673910B2
Source datasetuspto-grants-2014_03
ORD IDord-e31fc0529a614565a9fe1bbeada33c21
Source noteuspto-grants-2014_03