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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1860269Generated: October 25, 2026

Ethyl chloroacetate → Ethyl-5-[(hydroxyimino)methyl]-2-nitro-3-thiopheneacetate

https://huagongshe.com/reaction/1860269

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroacetateHCID 7751—
Reactant5-Nitro-2-thiophenecarboxaldehyde oximeHCID 350516—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethylformamideHCID 6228—
ProductEthyl-5-[(hydroxyimino)methyl]-2-nitro-3-thiopheneacetateHCID 8580189627.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06528653B2
Source datasetuspto-grants-2003_03
ORD IDord-3725d1bfa4d54d478308ee4da6cc06a7
Source noteuspto-grants-2003_03