HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → HCID 131713380, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | O-Xylene | HCID 7237 | — |
| Reactant | Chloranil | HCID 8371 | — |
| Reactant | HCID 20470557 | HCID 20470557 | — |
| Product | HCID 131713380 | HCID 131713380 | — |
Reaction Steps
A mixture of 1-[p-(β-butyloxyethyl)-phenyl]-4-(p-bromophenyl)-cyclohexene (XV) (55 g, 0.13 mol) obtained in Step H, chloranil (78.4 g, 0.32 mol) and xylene (624 ml) was heated and placed under reflux for 24 hours. After cooling, toluene (800 ml) was added, insoluble solid filtered off and toluene removed by concentrating the filtrate. The resulting raw crystals were recrystallized from ethyl acetate (50 ml) to obtain 4"-(β-butyloxyethyl)-4-bromoterphenyl (XV1) (29 g) having a melting point of 225.7°~227.0° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04431564 |
| Source dataset | uspto-grants-1984_02 |
| ORD ID | ord-9bef4165fb134bdc9e8d48dc3e9c7a30 |
| Source note | uspto-grants-1984_02 |