HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → HCID 86635767, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 66912535 | HCID 66912535 | — |
| Product | HCID 86635767 | HCID 86635767 | 68% |
Reaction Steps
To a solution of acetyl 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 up 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-(acetamido)-4-methoxybenzylsulfone in 68% yield. M.p. 220-223° C. NMR (DMSO-d6) δ 2.02(s, 2H), 3.84(s, 3H), 3.86(s, 6H), 3.88(s, 3H), 4.22 (s, 2H), 6.08(s, 2H), 7.09-7.12(d, 1H vinylic), 6.88-7.86(m, aromatic), 8.35(s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07598232B2 |
| Source dataset | uspto-grants-2009_10 |
| ORD ID | ord-4a6f1ee3eb014fe597eccb106cc0eb4b |
| Source note | uspto-grants-2009_10 |