Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22879Generated: October 25, 2026

Benzenesulfonamide, N-[(4-methoxyphenyl)methyl]-2-nitro- → Benzenesulfonamide, N-[(4-methoxyphenyl)methyl]-2-nitro-

https://huagongshe.com/reaction/22879

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonamide, N-[(4-methoxyphenyl)methyl]-2-nitro-HCID 796366—
Reactant4-[(2-Nitro-benzenesulfonylamino)-methyl]-benzoic acid tert-butyl esterHCID 69794415—
ProductBenzenesulfonamide, N-[(4-methoxyphenyl)methyl]-2-nitro-HCID 796366—
Product2-amino-N-(4-methoxy-benzyl)-benzenesulfonamideHCID 1133991—

Reaction Steps

When in the procedure of Example 17, Step (2), 4-[(2-nitro-benzenesulfonylamino)-methyl]-benzoic acid tert-butyl ester was replaced with N-(4-methoxy-benzyl)-2-nitro-benzenesulfonamide, the title compound 2-amino-N-(4-methoxy-benzyl)-benzenesulfonamide was obtained as a thick oil. 1H-NMR (CDCl3); δ 7.71 (dd, 1H), 7.07 (d, 2H), 6.78 (m, 4H), 4.93 (bt, 1H), 4.82 (bs, 2H), 3.95 (d, 2H), and 3.75 (s, 3H). MS: M+−1=291.0 Da Step (3): Synthesis of 2-Amino-5-bromo-N-(4-methoxy-benzyl)-benzenesulfonamide

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06849648B2
Source datasetuspto-grants-2005_02
ORD IDord-a1c0cd5e0a54433c8c51fba9e71b84e4
Source noteuspto-grants-2005_02