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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1532025Generated: November 3, 2026

Acetic Acid → HCID 21251137, compound

https://huagongshe.com/reaction/1532025

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantMethanolHCID 887—
Reactant2-Amino-2-methyl-1-propanolHCID 11807—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 10511031HCID 10511031—
ReactantSodium MethoxideHCID 10942334—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 21251137HCID 2125113752.2%

Reaction Steps

3-Ethoxy-4-methylisoxazole-5-carbonitrile (2.6 g, 17.1 mmol), 5.4 M NaOMe in MeOH (0.6 mL, 3.4 mmol) and EtOH (80 mL) was stirred at room temperature for 30 min. Acetic acid (2.2 mL, 39.3 mmol) and 2-amino-2-methylpropan-1-ol (1.8 mL, 18.8 mmol) were added, and the resulting mixture was boiled under reflux for 20 h. The reaction mixture was cooled, added water (100 mL) and extracted with EtOAc (3×100 mL). The organic extracts were washed with 1 M NaOH (50 mL), brine, dried (MgSO4) and evaporated in vacuo. The residue was dissolved in EtOH (60 mL), a solution of KOH (1.8 g, 32 mmol) in water (12 mL) was added, and the mixture was stirred at room temperature for 20 h. EtOH was removed in vacuo, water was added (80 mL) and the aqueous phase extracted with EtOAc (3×100 mL). The organic extracts were washed with brine, dried (MgSO4) and evaporated in vacuo. Flash chromatography (silica gel, eluent: EtOAc/heptane/triethylamine=75:25:1) gave crude title compound as a yellow oil (2.0 g, 52%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06200999B1
Source datasetuspto-grants-2001_03
ORD IDord-0e5c8d596fc84607891526ab4678cbf4
Source noteuspto-grants-2001_03