HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzylamine → HCID 178520063, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 20270297 | HCID 20270297 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178520063 | HCID 178520063 | — |
Reaction Steps
A solution of 5-[[3-(3-formylphenoxy)propyl]amino]-1-methyl-1H-1,2,4-triazole-3-methanol (532 mg) in ethanol (15 ml) was treated with benzylamine (5 ml) and stirred at room temperature for 1.5 h. The solution was treated with sodium borohydride (500 mg) and stirred at room temperature for 16 h. The mixture was evaporated, and the residue partitioned between 2N hydrochloric acid and ethyl acetate. The aqueous layer was washed with ethyl acetate, neutralised with potassium carbonate, and extracted with ethyl acetate. The combined extracts were dried and evaporated in vacuo to yield an oil. This oil was chromatographed on silica gel, using a mixture of methanol-ethyl acetate (1:1) to give the title compound as an oil (315 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04536508 |
| Source dataset | uspto-grants-1985_08 |
| ORD ID | ord-517518395ae64c3eabc0ca40b65987f5 |
| Source note | uspto-grants-1985_08 |