HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aluminium lithium hydride → 2,3-Dioleyloxypropylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | 2,3-Dioleyloxypropyl azide | HCID 86751853 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,3-Dioleyloxypropylamine | HCID 11039228 | 98% |
Reaction Steps
In 30 ml of tetrahydrofuran was suspended 75 mg (2 mmol) of lithium aluminum hydride. While this suspension was held under ice-cooling, 1.03 g (1.7 mmol) of 2,3-dioleyloxypropyl azide was added dropwise and the mixture was stirred for 30 minutes. Then, the mixture was further stirred at ambient temperature for 2 hours. At completion of the reaction, the reaction mixture was poured in ice-water and extracted with ether and the extract was washed with water, dried, and concentrated. The residue was subjected to column chromatography (silica gel/methylene chloride-methanol) to provide 0.98 g (98%) of the title compound as colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05705188 |
| Source dataset | uspto-grants-1998_01 |
| ORD ID | ord-c9b0093acbde4270a6a5b861a636c18c |
| Source note | uspto-grants-1998_01 |