HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → 2-(3-Morpholin-4-YL-propoxy)-benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Salicylaldehyde | HCID 6998 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-(3-Chloropropyl)morpholine | HCID 95834 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(3-Morpholin-4-YL-propoxy)-benzaldehyde | HCID 13795260 | — |
Reaction Steps
Salicylaldehyde (17 g) is treated first with 6.7 g of 50% sodium hydride in 110 ml of dimethylformamide and then with 92 ml of a 2 N toluene solution of N-(3-chloropropyl)morpholine. The mixture is heated at 105°-110° C. for 4 hours, cooled and poured into 300 ml of water. The product is extracted three times with ether. The extracts are combined, dried, concentrated on a rotary evaporator and the residue distilled to give 32.3 g of product as an oil, boiling point 155°-160° C. at 0.1-0.2 mm of Hg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04151354 |
| Source dataset | uspto-grants-1979_04 |
| ORD ID | ord-3813147e4d56433ea5d9617feb06058c |
| Source note | uspto-grants-1979_04 |