HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 7-Fluoro-1,2,3,4-tetrahydronaphthalen-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 4-(4-Fluorophenyl)butyryl chloride | HCID 23293594 | — |
| Solvent | Carbon Disulfide | HCID 6348 | — |
| Product | 7-Fluoro-1,2,3,4-tetrahydronaphthalen-1-one | HCID 10374764 | — |
Reaction Steps
To a mixture of aluminum chloride (66 g, 0.50 mol) in carbon disulfide (600 mL) was added dropwise a solution of 4-(4-fluorophenyl)butyryl chloride (75.3 g, 0.37 mole) in carbon disulfide (260 mL) keeping the internal temperature below 10° C. After refluxing for 0.5 h, the reaction mixture was poured into a mixture of concentrated HCl (50 mL) and ice water (800 mL). The mixture was filtered and extracted with diethyl ether. The diethyl ether extracts were dried and concentrated in vacuo to give crude 7-fluoro-1-tetralone. Vacuum distillation gave pure 7-fluoro-1-tetralone b.p., 83° C. at 0.3 mm Hg which solidified to a white solid (94%). m.p., 62°-64° C. (lit, J. Am. Chem. Soc., 89, 386, 1967; m.p., 63.5°-65.0° C.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05719186 |
| Source dataset | uspto-grants-1998_02 |
| ORD ID | ord-143baa4b53ae4f0f8c063ad988aa9d73 |
| Source note | uspto-grants-1998_02 |