HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → HCID 22414561, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | hydroxylamine-O-sulfonic acid | HCID 76284 | — |
| Reactant | 41963-21-7 | HCID 21833829 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | 1,1-Dimethoxyethyl(dimethyl)amine | HCID 87835 | — |
| Product | HCID 22414561 | HCID 22414561 | — |
Reaction Steps
A solution of 4-bromo-3-methylbenzenecarbothioamide (1.20 g) in dimethylacetamide dimethyl acetal (2 ml) and dichloromethane (30 ml) was stirred under nitrogen at room temperature for 7 h. The solvent was evaporated in vacuo to give a dark brown oil to which was added hydroxylamine-0-sulphonic acid (0.88 g), methanol (20 ml) and pyridine (0.83 ml) and the mixture stirred at room temperature under nitrogen for 16 h. After evaporation, aqueous potassium carbonate was added and the mixture was extracted with dichloromethane. The combined extracts were dried and evaporated to give a brown residue which was purified by column chromatography on silica eluting with hexane: ethyl acetate (4:1) to give the title compound as an orange solid (0.8 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05340810 |
| Source dataset | uspto-grants-1994_08 |
| ORD ID | ord-cfee844cb9f1405d8c3717a25ccb8c47 |
| Source note | uspto-grants-1994_08 |