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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1770814Generated: November 2, 2026

Potassium Carbonate → 5-Methyl-3-(4-aminophenoxymethyl)isoxazole

https://huagongshe.com/reaction/1770814

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantSodium DithioniteHCID 24489—
Reactant5-Methyl-3-(4-nitrophenoxymethyl)isoxazoleHCID 60594586—
SolventDichloromethane methanolHCID 21226129—
Product5-Methyl-3-(4-aminophenoxymethyl)isoxazoleHCID 6102831146%

Reaction Steps

The 5-methyl-3-(4-nitrophenoxymethyl)isoxazole (3, X═H) (2.59 g, 11.07 mmol) was dissolved in MeOH:CH2Cl2 (1:1, 600 mL). An aqueous solution of (77 mL) sodium hydrosulfite (11.93 g, 68.5 mmol) and K2CO3 (9.55 g, 69 mmol) was added dropwise under nitrogen for 30 min. The reaction was allowed to stir at room temperature for 2 h, and the organic solvents were removed under reduced pressure, diluted with water (200 mL), extracted with CH2Cl2 (3×300 mL), dried over anhydrous Na2SO4 and solvent was removed under reduced pressure. The resulting product was finally dried under high vacuum to afford 1.03 g (46%) of the 5-methyl-3-(4-aminophenoxymethyl)isoxazole (4, X═H). 1H NMR (CDCl3): δ 6.78 (d, 2H, J=8.7 Hz), 6.61 (d, 2H, J=8.4 Hz), 6.07 (s, 1H), 5.01 (s, 2H), 3.44 (s, 2H), 2.40 (s, 3H); LCMS (m/z): 205 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09248190B2
Source datasetuspto-grants-2016_02
ORD IDord-e3cf0e5f4ae24e7eacb08fb2a56d3d25
Source noteuspto-grants-2016_02