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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358082Generated: October 30, 2026

Sodium Hydroxide → 2-Tert-butoxycarbonylmethoxyimino-2-(1,2,5-thiadiazol-3-yl)acetic acid

https://huagongshe.com/reaction/358082

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant(1,2,5-Thiadiazol-3-yl)glyoxylic acidHCID 12906559—
Reactanttert-Butyl (aminooxy)acetateHCID 12919121—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-Tert-butoxycarbonylmethoxyimino-2-(1,2,5-thiadiazol-3-yl)acetic acidHCID 5374326991.9%

Reaction Steps

To a solution of (1,2,5-thiadiazol-3-yl)glyoxylic acid (6 g) in tetrahydrofuran (30 ml) and water (30 ml) was added tert-butoxycarbonylmethoxyamine (8.37 g) at ambient temperature. The mixture was adjusted to pH 4.5-5.0 with 4N aqueous sodium hydroxide and stirred at ambient temperature for 4 hours. The mixture was adjusted to pH 7.5 with 4N aqueous sodium hydroxide and washed with ethyl acetate (100 ml×2). The aqueous solution was acidified to pH 2.0 with 10% hydrochloric acid and extracted with ethyl acetate (100 ml×2). The organic layer was washed with an aqueous sodium chloride and dried over magnesium sulfate. The solution was evaporated in vacuo to give 2-tert-butoxycarbonylmethoxyimino-2-(1,2,5-thiadiazol-3-yl)acetic acid (syn and anti mixture) (10.02 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04464369
Source datasetuspto-grants-1984_08
ORD IDord-df38488b7e454b3bb34fad0e4d1dffcb
Source noteuspto-grants-1984_08