HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiourea → Ethyl 2-methoxyimino-2-(2-aminothiazol-4-yl)acetate hydrobromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | Butanoic acid, 4-bromo-2-(methoxyimino)-3-oxo-, ethyl ester | HCID 54053279 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 2-methoxyimino-2-(2-aminothiazol-4-yl)acetate hydrobromide | HCID 73668749 | — |
Reaction Steps
A solution of ethyl 2-methoxyimino-4-bromoacetoacetate (a mixture of syn and anti isomers) (17.4 g.) and thiourea (5.4 g.) in ethanol (100 ml.) was refluxed for 4 hours. The reaction mixture was allowed to stand in a refrigerator to precipitate crystals. The crystals were collected by filtration, washed with ethanol and dried to give ethyl 2-methoxyimino-2-(2-aminothiazol-4-yl)acetate hydrobromide (anti isomer) (9.5 g.). The filtrate and the washings were put together and concentrated under reduced pressure. Water (100 ml.) was added to the residue and the mixture was washed with ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04299829 |
| Source dataset | uspto-grants-1981_11 |
| ORD ID | ord-6d636eafaf48447bb21a71ac6646d0c3 |
| Source note | uspto-grants-1981_11 |