HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 21417396, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | [4-(Phenylethynyl)phenyl]methanol | HCID 15881239 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 21417396 | HCID 21417396 | — |
Reaction Steps
Thionyl chloride, 7 ml., is added dropwise to a stirred solution of 6.0 g. (0.0288 mole) of 4-(phenylethynyl) benzyl alcohol in 100 ml. of dry chloroform at room temperature and the mixture is stirred for 6 hours. Solvent is evaporated under reduced pressure and at a temperature below 50°. The residue is freed from traces of thionyl chloride by dissolution in dry benzene and evaporation under reduced pressure. This process is repeated and the residual solid product is purified by sublimation in vacuo; m.p. 61.5°-63.5°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03957871 |
| Source dataset | uspto-grants-1976_05 |
| ORD ID | ord-32c99f0901254f3e85902a397b9fcfba |
| Source note | uspto-grants-1976_05 |