HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 376339Generated: October 26, 2026
Triethylamine → 3-Phenylthio-4-(4-(methylsulfonyl)phenyl)-5h-furan-2-one
https://huagongshe.com/reaction/376339
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (Phenylthio)acetic acid | HCID 59541 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 2-Bromo-4'-(methylsulfonyl)acetophenone | HCID 735823 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-Phenylthio-4-(4-(methylsulfonyl)phenyl)-5h-furan-2-one | HCID 10269135 | — |
Reaction Steps
At 0° C., triethylamine (335 μL) was added to a solution of thiophenoxyacetic acid (161 mg) and 2-bromo-1-(4-(methylsulfonyl)phenyl) ethanone (272 mg, WO 9500501, example 9, Step 1) in 5 mL of acetonitrile and the mixture was stirred at 0° C. for 1 h. The reaction mixture was then cooled to -20° C. and DBU (265 μL) was added. The mixture was stirred for 30 min. at -20° C. and was quenched by addition of 1N HCl. The product was extracted with EtOAc, dried over sodium sulfate and partially purified by silica gel chromatography. The impure product was recrystalized from EtOAc/Hexane to afford the title compound as a solid
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06020343 |
|---|
| Source dataset | uspto-grants-2000_02 |
|---|
| ORD ID | ord-a7f933a414fb4257bb076908f26569f6 |
|---|
| Source note | uspto-grants-2000_02 |
|---|