HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 21283572, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 21283567 | HCID 21283567 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 21283572 | HCID 21283572 | — |
Reaction Steps
Thionyl chloride (0.78 cc) is added in the course of 10 minutes to a stirred solution, cooled beforehand to 0° C., of 3-phenyl-1-naphthalenemethanol (1 g) in chloroform (20 cc), and the temperature is then allowed to rise to room temperature (approximately 20° C.) The mixture is stirred for 15 hours at this temperature and the solvent evaporated under reduced pressure. 1-Cloromethyl-3-phenylnaphthalene (1.1 g) is obtained, the proton NMR spectrum of which, in deuterated chloroform, shows the following characteristics:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04788204 |
| Source dataset | uspto-grants-1988_11 |
| ORD ID | ord-72473b3196e343fc9bbe8456d2598f71 |
| Source note | uspto-grants-1988_11 |