HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Alcohol → N-Benzyl-4-methoxyaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Triphenyl phosphite | HCID 7540 | — |
| Reactant | P-Anisidine | HCID 7732 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-Benzyl-4-methoxyaniline | HCID 519413 | 83% |
Reaction Steps
369 parts of p-anisidine, 162 parts of benzyl alcohol and 15 parts of triphenyl phosphite are first heated to 177° C. At this temperature, the elimination of water commences. The condensation has ended after 5 hours, when the internal temperature is 231° C. 27 parts of water are removed. Excess p-anisidine and excess benzyl alcohol are distilled off under reduced pressure. 265 parts of N-benzyl-4-methoxy-aniline, corresponding to a yield of 83% of theory, distil at 190° C/5 mm Hg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04067903 |
| Source dataset | uspto-grants-1978_01 |
| ORD ID | ord-bede904dcaea4ab096ce933e0a926504 |
| Source note | uspto-grants-1978_01 |