HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Naphthol → 7,8,9,10-Tetrahydrobenzo[b]naphtho[2,1-d]furan
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Naphthol | HCID 7005 | — |
| Reactant | 1,3-Cyclohexadiene | HCID 11605 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 7,8,9,10-Tetrahydrobenzo[b]naphtho[2,1-d]furan | HCID 268555 | 25% |
Reaction Steps
144 g of 1-naphthol, 190 g of p-toluenesulfonic acid monohydrate, 80.1 g of 1,3-cyclohexadiene and 4 L of toluene were placed in a flask. The resulting mixture was stirred under reflux for 24 hours. After cooling to room temperature, the reaction solution was washed with 600 mL of water. After drying an organic phase with magnesium sulfate, the solvent was distilled off under reduced pressure. Residues were purified by silica gel column chromatography, whereby 55.5 g (yield: 25%) of 7,8,9,10-tetrahydrobenzo[b]naphtho[2,1-d]furan was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08629430B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-272f4450c6e64cd1a060c609e02625cb |
| Source note | uspto-grants-2014_01 |