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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 922242Generated: November 1, 2026

Methanol → Methyl 2-(3-methylisoxazol-5-yl)acetate

https://huagongshe.com/reaction/922242

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantThionyl ChlorideHCID 24386—
Reactant2-(3-Methyl-1,2-oxazol-5-yl)acetic acidHCID 4195532—
ProductMethyl 2-(3-methylisoxazol-5-yl)acetateHCID 1236687592%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a 50 mL RB flask fitted with magnetic stirrer was charged with 10 mL of methanol. To the stirred solvent was added (3-methyl-1,2-oxazol-5-yl)acetic acid (1 g, 7 mmol), was added drop wise SOCl2 (1.25 g, 10.5 mmol) to the reaction mixture at 0° C. and stirred at 50° C. for 4 h. After completion of the reaction, the reaction mixture was concentrated to distill off the solvent; water (25 mL) was added and extracted with ethyl acetate (25 mL). The organic layer was washed with saturated NaHCO3 solution (10 mL) and brine solution (10 mL). The organic layer was dried over anhydrous Na2SO4 and the solvent was removed under reduced pressure. The product was obtained as brown liquid (1 g, yield: 92%). 1H NMR (300 MHz, CDCl3): δ 6.03 (s, 1H), 3.73 (d, 2H), 3.69 (s, 3H), 2.23 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278915B2
Source datasetuspto-grants-2016_03
ORD IDord-72bdaca1cb1d4376b22829b5a30417bf
Source noteuspto-grants-2016_03