HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → 1-(2,5-Dimethylphenyl)-1-(2-benzyloxyphenyl)-propan-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1-(2,5-Dimethylphenyl)propan-1-one | HCID 3614648 | — |
| Reactant | HCID 178419625 | HCID 178419625 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(2,5-Dimethylphenyl)-1-(2-benzyloxyphenyl)-propan-1-ol | HCID 20207214 | — |
Reaction Steps
To 100 ml. of a 1.5 molar solution of 2-benzyloxyphenyl magnesium bromide in tetrahydrofurane a solution of 24.3 g. of 2',5'-dimethyl-propiophenone in 50 ml. of dry tetrahydrofurane is added under moderate reflux. The reaction mixture is stirred under slight boiling for 30 minutes, cooled and poured onto a saturated solution of ammonium chloride in ice water. Tetrahydrofurane is distilled off under reduced pressure, and the residue is extracted with benzene. The benzene phase is washed to neutral with water, and dried over anhydrous sodium sulfate. The benzene is evaporated in vacuo and the residue is fractionated to yield 43.9 g. of the named compound, boiling at 160°-162° C./1.33 Pa.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04605785 |
| Source dataset | uspto-grants-1986_08 |
| ORD ID | ord-f5f4df7e37544156b93ad968980c8ddd |
| Source note | uspto-grants-1986_08 |