HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 918350Generated: November 2, 2026
Diisopropylamine → HCID 53748142, compound
https://huagongshe.com/reaction/918350
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Reactant | n-Dodecylformamide | HCID 244441 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 53748142 | HCID 53748142 | — |
Reaction Steps
A solution of 213 g of dodecylformamide (1.0 mole) in 500 ml of anhydrous benzene is added dropwise at 20°-30° to a suspension of 208 g of phosphorus pentachloride (1.0 mole) in 750 ml of anhydrous benezne. After a further 12 hours of stirring at 30°, the reaction mixture is concentrated in vacuo to dryness. The residue is then dissolved in 100 ml of anhydrous benzene, and 202 g of di-isopropylamine (2.0 moles) added dropwise at 40°-50°. The whole is heated for 2 hours at 50°; water and ice are added, and the mixture rendered alkaline with aqueous sodium hydroxide solution. The organic layer is then separated and concentrated by evaporation. The N1,N 1 -diisopropyl-N2 -dodecyl-formamidine obtained as residue boils at 125°-128°C and 0.03 Torr.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US03971647 |
|---|
| Source dataset | uspto-grants-1976_07 |
|---|
| ORD ID | ord-75dbf75339164729b1bbe151e37d3ef5 |
|---|
| Source note | uspto-grants-1976_07 |
|---|