HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Methoxyaniline → HCID 835338, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Methoxyaniline | HCID 10824 | — |
| Reactant | HCID 779038 | HCID 779038 | — |
| Reactant | HCID 819756 | HCID 819756 | — |
| Product | HCID 835338 | HCID 835338 | 73% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08673910B2 |
| Source dataset | uspto-grants-2014_03 |
| ORD ID | ord-e31fc0529a614565a9fe1bbeada33c21 |
| Source note | uspto-grants-2014_03 |