HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 544671Generated: October 31, 2026
Hydrochloric Acid → Ethyl 9,10-dihydrophenanthrene-1-carboxylate
https://huagongshe.com/reaction/544671
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | Ethyl 2-[2-(2-aminophenyl)ethenyl]benzoate | HCID 53977807 | — |
| Catalyst | Copper Sulfate | HCID 24462 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 9,10-dihydrophenanthrene-1-carboxylate | HCID 13281335 | 43.6% |
Reaction Steps
To a stirred solution of ethyl 2-[2-(2-aminophenyl)ethenyl]benzoate (13.5 grams, 0.05 mole) in warm glacial acetic acid (75 ml) was added a solution of concentrated hydrochloric acid (12 ml) in water (10 ml). The mixture was cooled to 0°, and during a 20 minute period a solution of sodium nitrite (3.7 grams, 0.054 mole) in water (30 ml) was added. The resultant mixture was stirred at 0°-5° for three hours. During a 90 minute period the mixture was added to a refluxing solution of copper sulfate (35 grams, 0.14 mole) in water (500 ml). After complete addition, glacial acetic acid (40 ml) was added and the mixture refluxed for one hour. The mixture was cooled to room temperature and extracted with three 200 ml portions of methylene chloride. The extracts were combined, washed with water, and evaporated under reduced pressure to give a brown oil. Distillation of the oil under reduced pressure gave ethyl 9,10-dihydrophenanthrene-1-carboxylate (5.5 grams, bp 145°-165°/0.25 mm) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04451484 |
|---|
| Source dataset | uspto-grants-1984_05 |
|---|
| ORD ID | ord-9e4f3d0d6aec49d7b10d13d44e2e9e33 |
|---|
| Source note | uspto-grants-1984_05 |
|---|