HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethyl phosphite → 5H-benzofuro[3,2-c]carbazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethyl phosphite | HCID 31215 | — |
| Reactant | HCID 66797872 | HCID 66797872 | — |
| Solvent | 1,2-Dichlorobenzene | HCID 7239 | — |
| Product | 5H-benzofuro[3,2-c]carbazole | HCID 66585341 | — |
Reaction Steps
20 g of 4-(2-nitrophenyl)dibenzofuran (69 mmol) and 48 ml of triethyl phosphite (276 mmol) are heated at the boil in 800 ml of 1,2-dichlorobenzene under a protective-gas atmosphere for 48 h. After this time, the remaining triethyl phosphite and the 1,2-dichlorobenzene are removed by distillation. The residue which remains is recrystallised from heptane/ethyl acetate. The yield is 13 g (45 mmol, 65%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09126970B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-1983fe9222d5478da712ec9662ef704c |
| Source note | uspto-grants-2015_09 |