Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2408364Generated: November 1, 2026

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

https://huagongshe.com/reaction/2408364

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 numberUS08815848B2
Source datasetuspto-grants-2014_08
ORD IDord-ce90600124af4b71baeeb03280a6fad3
Source noteuspto-grants-2014_08