HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Chloride → Benzyl Phenyl Ether
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | Sodium Phenoxide Trihydrate | HCID 23681143 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Benzyl Phenyl Ether | HCID 70352 | 67% |
Reaction Steps
A mixture of sodium phenolate trihydrate (10.2 g; 60 mmole) and benzyl chloride (6.4 ml; 56 mmole) in methanol (150 ml) was pumped through the system (15 ml/minute; 146°-7° C.; 1000-1050 kPa). The MeOH was rotary evaporated off and the residue recrystallised from EtOH to afford colourless needles of phenyl benzyl ether (6.9 g; 67% yield), m.p. 36°-36.3° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05387397 |
| Source dataset | uspto-grants-1995_02 |
| ORD ID | ord-80ea20519fd44352987956fe78cc4b12 |
| Source note | uspto-grants-1995_02 |