HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 21439984, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Ethyl {3-chloro-4-[(1,3-thiazol-2-yl)amino]phenyl}acetate | HCID 21439966 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21439984 | HCID 21439984 | — |
Reaction Steps
A mixture of ethyl 2-[3-chloro-4-(N-thiazol-2-ylamino)phenyl]acetate (8.9 g), methyl iodide (44 ml) and ethanol (44 ml) is heated at 50°-55° C for 42 hours with stirring. The ethanol and methyl iodide are evaporated and the residue is washed with ether and kept at room temperature to give a precipitate. The precipitate is washed with ethyl acetate and cold acetone successively and recrystallized from acetone to give 3-methyl-2-[2-chloro-4-(ethoxycarbonylmethyl)anilino]-thiazolium iodide (6.6 g) melting at 147°-148° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04018785 |
| Source dataset | uspto-grants-1977_04 |
| ORD ID | ord-f30265a530be464a98fbcf78e75a3aed |
| Source note | uspto-grants-1977_04 |