HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1269345Generated: October 25, 2026
Rofecoxib → (2Z)-2-[4-(methylsulfonyl)phenyl]-3-phenylbut-2-ene-1,4-diol
https://huagongshe.com/reaction/1269345
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Rofecoxib | HCID 5090 | — |
| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (2Z)-2-[4-(methylsulfonyl)phenyl]-3-phenylbut-2-ene-1,4-diol | HCID 57434773 | 98.7% |
Reaction Steps
To a solution of 110 g of 4-(4-methanesulfonyl-phenyl)-3-phenyl-5H-furan-2-one in 1.5 L of dichloromethane stirred at −78° C., 150 mL of DIBAL was added dropwise. The resulting mixture was warmed to room temperature and stirred overnight. The reaction mixture was then cooled to −78° C., and 1.2 L of 1 M aqueous NaOH was added dropwise. After the addition, the resulting mixture was warmed to room temperature and the organic phase was separated. The aqueous phase was extracted with dichloromethane. The organic phases were combined and dried over Na2SO4. 110 g of the titled compound was obtained after evaporation. 1H NMR (acetone-d6, 500 M Hz): δ 7.69 (d, 2 H), 7.36 (d, 2 H), 7.16–7.05 (m, 5 H), 4,66 (d, 2 H), 4.63 (d, 2 H), 4.19 (t, 1 H, OH), 4.17 (t, 1 H. OH), 3.04 (s, 3 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07199154B2 |
|---|
| Source dataset | uspto-grants-2007_04 |
|---|
| ORD ID | ord-a0d1798d1a4a4937b9d1bbf49333574c |
|---|
| Source note | uspto-grants-2007_04 |
|---|