HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 2-(dimethoxymethyl)-5-methyl-4-(trifluoromethyl)-1H-imidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | Acetaldehyde, 2,2-dimethoxy- | HCID 162650 | — |
| Reactant | 2,2,2-Trifluoro-1-(2-methyl-1,3-dithian-2-yl)ethanone | HCID 86648480 | — |
| Catalyst | Silver Nitrate | HCID 24470 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-(dimethoxymethyl)-5-methyl-4-(trifluoromethyl)-1H-imidazole | HCID 67549218 | — |
Reaction Steps
NCS (870 mg, 6.51 mmol) and silver nitrate (1.48 g, 8.71 mmol) were dissolved in acetonitrile (40 mL) and distilled water (10 mL). 2,2,2-Trifluoro-1-(2-methyl-1,3-dithian-2-yl)ethanone obtained in Example (36a) (500 mg, 2.17 mmol) was added, and the mixture was stirred for 40 minutes. Thereafter, dimethoxyacetaldehyde (5.76 M aqueous solution, 0.4 mL, 23.0 mmol) and 28% aqueous ammonia (2 mL) were added, and the mixture was stirred at room temperature for 18 hours. The reaction solution was filtered through celite and then concentrated under reduced pressure. The resulting compound was used for the next reaction without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08927588B2 |
| Source dataset | uspto-grants-2015_01 |
| ORD ID | ord-671107ff5f2c4dceb2710698bd8a9fe9 |
| Source note | uspto-grants-2015_01 |