Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Phenylacetic Acid | HCID 999 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 2-Bromo-4'-(methylsulfonyl)acetophenone | HCID 735823 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Rofecoxib | HCID 5090 | — |
Reaction Steps
To a solution of phenylacetic acid (27.4 g, 201 mmol) and 2-bromo-1-(4-(methylsulfonyl)phenyl)ethanone (Example 1, Step 1)(60 g, 216 mmol, 1.075 eq.) in acetonitrile (630 mL) at 25° C. was added slowly Et3N (30.8 mL, 1.1 eq.). The mixture was stirred for 20 min. at room temperature and then cooled in an ice bath. DBU (60.1 mL, 3 eq.) was slowly added. After stirring for 20 min. in the ice bath, the reaction was complete and the mixture was acidified with 1N HCl (color changes from dark brown to yellow). Then 2.4 L of ice and H2O were added, stirred for a few minutes, then the precipitate was filtered and rinsed with H2O (giving 64 g of crude wet product). The solid was dissolved in 750 mL of CH2Cl2 (dried over MgSO4, filtered) and 300 g of silica gel was added. The solvent was evaporated to near dryness (silica gel a bit sticky) and the residue was applied on top of a silica gel plug (sintered glass funnel), eluted with 10% EtOAc/CH2Cl2, giving, after evaporation of the solvent and swishing in EtOAC, 36.6 g (58%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05663195 |
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| Source dataset | uspto-grants-1997_09 |
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| ORD ID | ord-6eb78a90e92345b1b9f8ffa701083e54 |
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| Source note | uspto-grants-1997_09 |
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