HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phosphoric Acid → 4,5,6,7-Tetrahydro-4-oxothionaphthene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phosphoric Acid | HCID 1004 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 4-(2-Thienyl)Butyric Acid | HCID 78386 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4,5,6,7-Tetrahydro-4-oxothionaphthene | HCID 83418 | 88.9% |
Reaction Steps
4-(2-Thienyl)butyric acid (28.42 g, 167 mmol) was placed in a round bottom flask with acetic anhydride (30 mL) and phosphoric acid (0.6 mL), and heated to reflux for 3.2 hours. The reaction mixture was poured into 100 mL of water, extracted with ethyl acetate, washed with brine, dried over MgSO4, and concentrated in vacuo to give a brown oil (22.60 g) which was vacuum distilled (1 mm Hg, 107°-115° C.) to give a white solid (13.08 g, 51%): mp 34°-40° C.); 1H NMR (CDCl3) 300 MHz 7.29 (d, J=5.2 Hz, 1H), 6.99 (d, J=5.2 Hz, 1H, 2.95 (t, J=6.0 Hz, 2H), 2.47(m, 2H), 2.13(m, 2H). M+H=153.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05760068 |
| Source dataset | uspto-grants-1998_06 |
| ORD ID | ord-efcca95a23374a6c92307a68aa24f83c |
| Source note | uspto-grants-1998_06 |