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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539652Generated: October 23, 2026

Hydrochloric Acid → Tert-butyl 1,3-thiazole-4-carboxylate

https://huagongshe.com/en/reaction/539652

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactanttert-ButanolHCID 6386—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant4-Thiazolecarboxylic acidHCID 304271—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductTert-butyl 1,3-thiazole-4-carboxylateHCID 1674429447%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of thiazole-4-carboxylic acid 7.1 (1 g, 7.2 mmol) and carbonyldiimidazole (6.3 g, 38.7 mmol) in commercial dry DMF (50 mL) under N2 was stirred at 50° C. for 20 min. Tert-butanol (8.6 g, 116.0 mmol) and DBU (5.8 mL, 38.7 mmol) were then successively added at once and the reaction was warmed at 60° C. for 48 h. The RM was then allowed to cool down to RT and the pH was adjusted to 4 with a solution of HCl (2M, ˜80 mL). The mixture was diluted with water (250 mL) and extracted with Et2O (3×100 mL). The combined org. layers were washed with brine (250 mL), dried over MgSO4, concentrated and purified on silica gel using DCM to afford title product as yellowish oil (47%). Yield: 3.37 g (47%). LCMS: P=98%, rt=3.65 nm, m/z=186.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871761B2
Source datasetuspto-grants-2014_10
ORD IDord-beb5a80539924462b21bb4ef310f3bf3
Source noteuspto-grants-2014_10