HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → HCID 178419054, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | (Phenylmethoxy)acetaldehyde | HCID 108989 | — |
| Reactant | Butanal, 2,2-dichloro-3-methyl- | HCID 9942197 | — |
| Product | HCID 178419054 | HCID 178419054 | — |
Reaction Steps
In 200 ml of acetonitrile was dissolved 53 g (339 mmol) of 2,2-dichloro-3-methylbutyraldehyde (1). Then, at 0° C., 45 g of benzyloxyacetaldehyde (2c)and 400 ml of aqueous ammonia (28%)were added. The mixture was stirred at room temperature for 15 hours. This reaction mixture was concentrated under reduced pressure and the residue was extracted with methylene chloride. The extract was washed with saturated brine, dried over sodium sulfate, and filtered. The filtrate was concentrated under reduced pressure to provide 2-(benzyloxymethyl)-4-isopropyl-1H-imidazole (3c). Yield 77 g (98.5%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05910506 |
| Source dataset | uspto-grants-1999_06 |
| ORD ID | ord-0e138f96405c4668a040ec284cfc2be3 |
| Source note | uspto-grants-1999_06 |