HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1979690Generated: October 29, 2026
Methanol → alpha-Methoxyimino-alpha-(5-chloro-2-benzothienyl)acetic acid
https://huagongshe.com/reaction/1979690
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | HCID 54377917 | HCID 54377917 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | alpha-Methoxyimino-alpha-(5-chloro-2-benzothienyl)acetic acid | HCID 53750490 | — |
Reaction Steps
A solution of 2.6 g of methylthio α-oxo-α-(5-chloro-2-benzothienyl)acetate in 180 ml of methanol containing 840 mg of hydroxylamine hydrochloride and 10 ml of 1N sodium hydroxide was stirred at 25° C. for sixteen hours. The reaction solvent was removed by evaporation under reduced pressure to give an oil. The oil was dissolved in 100 ml of ethyl acetate and 100 ml of water, and the mixture was made alkaline to pH 10.4 by addition of 1N sodium hydroxide. The aqueous layer was separated, washed with fresh ethyl acetate, and then made acidic to pH 2 by addition of 1N hydrochloric acid. The aqueous acid mixture was extracted with fresh ethyl acetate, which was then washed with water, dried and the solvent was removed to provide 2.5 g of α-methoxyimino-α-(5-chloro-2-benzothienyl)acetic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04482553 |
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| Source dataset | uspto-grants-1984_11 |
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| ORD ID | ord-80f53a16db8c4cd198fca567b319e0bc |
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| Source note | uspto-grants-1984_11 |
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