HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethyl phosphite → HCID 14949160, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethyl phosphite | HCID 31215 | — |
| Reactant | 1H-Indene, 2-bromo- | HCID 575586 | — |
| Catalyst | Nickel Dichloride | HCID 24385 | — |
| Product | HCID 14949160 | HCID 14949160 | — |
Reaction Steps
To 91.0 g (0.467 mol) of 2-bromo-1H-indene and 3.02 g (0.023 mol) of NiCl2 in 250 ml flask equipped with a distillation head, 85.0 ml (82.4 g, 0.496 mol) of (EtO)3P were added. This black mixture was heated in the oil bath at 185–190° C. for 3 hours. During this procedure, argon gas was bubbled through the mixture to eliminate ethyl bromide formed. The crude product was distilled in vacuum (171–175° C./1 mm). Yield 102.4 g (87%) of colorless oil of diethyl 1H-inden-2-ylphosphonate, 9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07214746B2 |
| Source dataset | uspto-grants-2007_05 |
| ORD ID | ord-7915c681c5c741098d5571d5eaf05167 |
| Source note | uspto-grants-2007_05 |