HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromotriphenylmethane → HCID 54369513, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromotriphenylmethane | HCID 11692 | — |
| Reactant | HCID 68144007 | HCID 68144007 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 54369513 | HCID 54369513 | — |
Reaction Steps
A mixture of .06 mole of sodium 5-cyano-2-methyl-1-(p-methylsulfinylbenzylidene)-3-indenylacetate and 0.05 mole of trityl bromide in 100 ml. anhydrous benzene is refluxed with rapid stirring under nitrogen for 5 hours. The hot reaction mixture is filtered and the filtrate is concentrated in vacuo. The residue is recrystallized from methyl ethyl ketone to give trityl 5-cyano-2-methyl-1-(p-methylsulfinylbenzylidene)-3-indenylacetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03956363 |
| Source dataset | uspto-grants-1976_05 |
| ORD ID | ord-12ec34270fc9482e82a68c83a0f3c119 |
| Source note | uspto-grants-1976_05 |