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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1723587Generated: October 31, 2026

Methanol → 2-Cyclopropyloxyimino-2-(5-tritylamino-1,2,4-thiadiazol-3-yl)acetic acid

https://huagongshe.com/reaction/1723587

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 2-cyclopropyloxyimino-2-(5-tritylamino-1,2,4-thiadiazol-3-yl)acetateHCID 53744924—
SolventTetrahydrofuranHCID 8028—
Product2-Cyclopropyloxyimino-2-(5-tritylamino-1,2,4-thiadiazol-3-yl)acetic acidHCID 5418567874.7%

Reaction Steps

A solution of ethyl 2-cyclopropyloxyimino-2-(5-tritylamino-1,2,4-thiadiazol-3-yl)acetate (syn isomer)(11 g) in a mixture of tetrahydrofuran (72 ml), methanol (72 ml) and 2N sodium hydroxide (72 ml) was stirred at ambient temperature overnight. The mixture was concentrated in vacuo. The residue was dissolved in a mixture of ethyl acetate and water and adjusted to pH 2 with 3N hydrochloric acid. The organic layer wad separated, washed with water and saturated aquious solution of sodium chloride, dried over magnesium sulfate, concentrated in vacuo, and triturated with petrolium ether to give 2-cyclopropyloxyimino-2-(5-tritylamino-1,2,4-thiadiazol-3-yl) acetic acid (syn isomer) (7.75 g) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04861769
Source datasetuspto-grants-1989_08
ORD IDord-2fb0e690f22146ab960d5e067ec40bb0
Source noteuspto-grants-1989_08