HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl chloroacetate → Ethyl-5-[(hydroxyimino)methyl]-2-nitro-3-thiopheneacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl chloroacetate | HCID 7751 | — |
| Reactant | 5-Nitro-2-thiophenecarboxaldehyde oxime | HCID 350516 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl-5-[(hydroxyimino)methyl]-2-nitro-3-thiopheneacetate | HCID 85801896 | 27.1% |
Reaction Conditions
| Temperature | -30 °C |
|---|
Reaction Steps
Potassium tertiary-butoxide (960 mg, 8.6 mmol) was dissolved in N,N-dimethylformamide (10 ml) and the solution cooled to −30° C. A solution of 5-nitro-2-thiophenecarboxaldehyde oxime (400 mg, 2.86 mmol) and ethyl chloroacetate (356 mg, 2.86 mmol) was added dropwise in dry N,N-dimethylformamide (5 ml) over 5 minutes. The reaction mixture was stirred at −30° C. for 30 minutes then quenched with 2M HCl (50 ml), diluted with ethyl acetate, washed with water, dried over magnesium sulfate and evaporated to dryness. The residue was chromatographed on silica gel using hexane/diethyl ether (1:2) as eluent to give 200 mg of ethyl-5-[(hydroxyimino)methyl]-2-nitro-3-thiopheneacetate as a tan solid. MS(ES): m/e 227 [M+H].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06528653B2 |
| Source dataset | uspto-grants-2003_03 |
| ORD ID | ord-3725d1bfa4d54d478308ee4da6cc06a7 |
| Source note | uspto-grants-2003_03 |