HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Nitrobenzoyl chloride → HCID 86598615, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Nitrobenzoyl chloride | HCID 8502 | — |
| Reactant | HCID 66912535 | HCID 66912535 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86598615 | HCID 86598615 | 72% |
Reaction Steps
To a solution of 4-nitrobenzoyl chloride (10 mmol) in tetrahydrofuran (40 mL) was added dropwise a solution of 2,4,6-trimethoxystyryl-3-amino-4-methoxybenzylsulfone (10 mmol) in tetrahydrofuran. The solution was stirred overnight and the completion of the reaction was monitored by TLC. The solvent was removed and the residue was taken in dichloromethane and washed with water. The organic layer was dried over anhydrous sodium sulfate and evaporated to give (E)-2,4,6-trimethoxystyryl-3-(4-nitrobenzamido)-4-methoxybenzylsulfone in 72% yield. m.p. 206-208° C. NMR (DMSO-d6) δ 3.80(s, 3H), 3.81(s, 6H), 3.83(s, 3H), 4.18(s, 2H), 6.08(s, 2H), 7.14-7.23(d, 1H vinylic), 6.97-7.86(m, aromatic), 9.05(s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07598232B2 |
| Source dataset | uspto-grants-2009_10 |
| ORD ID | ord-bae92dcb78ac4aedaae89e7b263fa1cf |
| Source note | uspto-grants-2009_10 |