HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 4-[[Bis(p-dimethylaminophenyl)methoxy]acetyl]Morpholine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Dimethyl Ether | HCID 8254 | — |
| Reactant | 1,1,3,3-Tetramethylguanidine | HCID 66460 | — |
| Reactant | 4,4'-Bis(dimethylamino)benzhydrol | HCID 92742 | — |
| Catalyst | Methanesulfonic Acid | HCID 6395 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 4-[[Bis(p-dimethylaminophenyl)methoxy]acetyl]Morpholine | HCID 20488036 | — |
Reaction Steps
A solution of 4,4'-bis(N,N-dimethylamino)benzhydrol, methyl ether (9.0 g, 0.032 mole), glycol morpholinamide (4.6 g, 0.032 mole), 150 ml of tetrahydrofuran, 250 ml of n-hexane and 4 drops of methanesulfonic acid was refluxed for about 8 hours, during which time an additional 200 ml of solvent was added. The volume was reduced to 200 ml and the color was discharged with tetramethylguanidine. The solution was filtered hot and then cooled to precipitate a white solid. The solid was recrystallized from 350 ml of methyl cyclohexane to give 4.9 g of blue crystals; mp 147.8°-150° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04343939 |
| Source dataset | uspto-grants-1982_08 |
| ORD ID | ord-aedb3f7bf82141bca0c692617ca9a875 |
| Source note | uspto-grants-1982_08 |