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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1018129Generated: October 30, 2026

Hydrochloric Acid → HCID 178521499, compound

https://huagongshe.com/reaction/1018129

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 178476495HCID 178476495—
SolventDimethylformamideHCID 6228—
ProductHCID 178521499HCID 17852149931.5%

Reaction Steps

At 20° C., 5.28 g (0.02 mol) of 2-(3-hydroxyimino-3H-benzofuran-2-ylideneaminooxy)-ethyl acetate (XVI-1) in 20 ml of dimethylformamide are stirred with 4.24 g (0.048 mol) of 45% strength aqueous sodium hydroxide solution for 3 hours. The mixture is acidified with 2 N hydrochloric acid and extracted with ethyl acetate, the organic phase is dried over sodium sulphate and the solvent is distilled off under reduced pressure. According to HPLC analysis, the crude product contains 23.4% of the stereoisomer A and 4.1% of the stereoisomer B of benzofuran-2,3-dione2-[O-(2-hydroxy-ethyl)-oxime]3-oxime (X-1). Stirring the crude product with diethyl ether affords 1.4 g (28.5% of theory) of crystalline benzofuran-2,3-dione2-[O-(2-hydroxy-ethyl)-oxime]3-oxime (X-1) consisting of 84.7% of stereoisomer A and 6% of stereoisomer B (HPLC).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06479675B1
Source datasetuspto-grants-2002_11
ORD IDord-8b8ecc732aec449bac3246612d8b5f71
Source noteuspto-grants-2002_11