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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186642Generated: October 31, 2026

P-Anisidine → N-(4-methoxyphenyl)-4-nitrobenzenesulfonamide

https://huagongshe.com/reaction/1186642

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-AnisidineHCID 7732—
ReactantHCID 779038HCID 779038—
ProductN-(4-methoxyphenyl)-4-nitrobenzenesulfonamideHCID 750280—

Reaction Steps

(RK1-1-27E) I This compound was prepared according to the procedure described for compound 11a except using p-anisidine to obtain the required product as a light brown solid. (278 mg, 100%) Mp=173-175° C. (lit 187-189° C., Tetrahedron 62(25), 6100-6106; 2006); 1H NMR (400 MHz, CDCl3) δ 8.28 (d, J=8.8 Hz, 2H), 7.85 (d, J=8.8 Hz, 2H), 6.97 (d, J=9.0 Hz, 2H), 6.80 (d, J=9.0 Hz, 2H), 6.36 (br s, 1H), 3.78 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673910B2
Source datasetuspto-grants-2014_03
ORD IDord-42280d90cb53465a883d5872e8d13800
Source noteuspto-grants-2014_03