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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570196Generated: November 1, 2026

Pivalaldehyde → Methyl 3-tert-butylisoxazole-5-carboxylate

https://huagongshe.com/reaction/570196

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPivalaldehydeHCID 12417—
ReactantMethyl propiolateHCID 13536—
ReactantChlorosuccinimideHCID 31398—
ReactantHydroxylamine monohydrateHCID 22235265—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductMethyl 3-tert-butylisoxazole-5-carboxylateHCID 15812234—

Reaction Steps

Pivaldehyde (1.10 mL, 10.0 mmol) was dissolved in dry DMF (10 mL), and NH2OH.H2O (0.590 mL of 55 wt % aqueous solution, 10.5 mmol) was added via syringe. The resulting mixture was stirred at room temperature for 4 h, NCS (1.40 g, 10.5 mmol) was added in small portions, and the resulting mixture was stirred at room temperature for 1 h. CuSO4.5H2O (75.0 mg, 0.300 mmol), methyl propiolate (1.07 mL, 12.0 mmol), and H2O (5 mL) were added followed by Cu powder (25.0 mg, 0.393 mmol). The resulting mixture was stirred at room temperature for 16 h and quenched with dilute aqueous NH4OH (2 mL). The aqueous solution was extracted with hexanes (3×30 mL), and then the combined organic extracts were dried over MgSO4 and filtered. The solvent was removed under reduced pressure to yield the title compound as a colorless oil. 1H-NMR (400 MHz, CDCl3) δ: 6.88 (s, 1H), 3.96 (s, 3H), 1.36 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09023846B2
Source datasetuspto-grants-2015_05
ORD IDord-28cbfbe88bea40c7a07d8cc58a63da06
Source noteuspto-grants-2015_05