HuagongsheHuagongshe Chemistry Print Report · For research reference only
N,N-Dimethylaniline → Ethyl alpha-methoxyimino-[2-(beta,beta,beta-trichloroethoxycarbonylamino)thiazol-4-yl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N,N-Dimethylaniline | HCID 949 | — |
| Reactant | 2,2,2-Trichloroethyl carbamothioylcarbamate | HCID 13092037 | — |
| Reactant | Butanoic acid, 4-bromo-2-(methoxyimino)-3-oxo-, ethyl ester | HCID 54053279 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl alpha-methoxyimino-[2-(beta,beta,beta-trichloroethoxycarbonylamino)thiazol-4-yl)acetate | HCID 54457368 | — |
Reaction Steps
To a solution of 2.2 g. of ethyl α-methoxyimino-β-oxo-γ-bromobutyrate in 40 ml. of ethanol are added 1.22 g. of dimethylaniline and 2.2 g. of N-(β,β,β-trichloroethoxycarbonyl)thiourea. The mixture is heated for 1.5 hours under reflux and concentrated under reduced pressure. The concentrate of the reaction mixture is recrystallized from ligroin to give ethyl α-methoxyimino-[2-(β,β,β-trichloroethoxycarbonylamino)thiazol-4-yl]acetate as crystals. 1.84 g. Melting point: 125°-128° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04355160 |
| Source dataset | uspto-grants-1982_10 |
| ORD ID | ord-3f76498cb980435e8d1d123a6e87df39 |
| Source note | uspto-grants-1982_10 |