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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1971690Generated: October 25, 2026

Hydrochloric Acid → 2-(Tert-butyl-(2-(3-(thiazol-5-yl)prop-2-ynyloxy)ethyl)amino)-2-oxoacetic acid

https://huagongshe.com/reaction/1971690

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium HydroxideHCID 14797—
ReactantEthyl 2-(tert-butyl(2-(3-(thiazol-5-yl)prop-2-ynyloxy)ethyl)amino)-2-oxoacetateHCID 58124907—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product2-(Tert-butyl-(2-(3-(thiazol-5-yl)prop-2-ynyloxy)ethyl)amino)-2-oxoacetic acidHCID 58124930104.2%

Reaction Conditions

Temperature55 °C

Reaction Steps

A solution of 450 mg of 11e in 4 ml of dioxane was mixed with a solution of 250 mg of KOH in 2 ml of water and stirred at 55° C. for 1 h. The reaction mixture was then cooled and diluted with 20 ml of water and made acidic to pH3 by addition of 0.5N HCl. The product was extracted with ethyl acetate. The organic extract was washed once with water, dried and concentrated, to give 430 mg of 11f as a colorless oil, which solidified on standing; Mp: 104-105° C.; Rf 0.20 (CH2Cl2/methanol 8/2). MS-ESI:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431564B2
Source datasetuspto-grants-2013_04
ORD IDord-621bc18995544258bd6561c06d149bd1
Source noteuspto-grants-2013_04