HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aminoacetaldehyde dimethyl acetal → HCID 69993910, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aminoacetaldehyde dimethyl acetal | HCID 89728 | — |
| Reactant | 1-[4-[(6-Bromohexyl)oxy]butyl]benzene | HCID 11012439 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 69993910 | HCID 69993910 | 32.3% |
Reaction Steps
To a solution of 8.7 ml (79.85 mmol) aminoacetaldehyde dimethylacetal in 60 ml toluene at reflux is added dropwise a solution of 10 g (31.94 mmol) 4-(6-bromohexyloxy)butylbenzene in 40 ml toluene. After maintaining the reaction mixture under reflux for 4 hr, toluene is evaporated off under reduced pressure, and 50 ml CH2Cl2 is added thereto. The resulting solution is stirred for 15 min together with a solution of 20 ml 47% HBr diluted with 20 ml H2O. The reaction mixture is allowed to decant and the crude product obtained as a result of evaporating the CH2Cl2 phase to dryness is triturated with Et2O and filtered, thereby affording 4.31 g (32.3%) N-dimethoxyethyl-6-(4-phenylbutoxy)hexylamine hydrobromide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06388134B1 |
| Source dataset | uspto-grants-2002_05 |
| ORD ID | ord-621dfefb25d945e6ac6e25888e0824b6 |
| Source note | uspto-grants-2002_05 |