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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1807536Generated: November 1, 2026

Triethylamine → (3-Isobutoxy-5-methyl-isoxazol-4-yl)-methanol

https://huagongshe.com/reaction/1807536

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
ReactantSodium borohydrideHCID 4311764—
Reactant3-Isobutoxy-5-methyl-isoxazole-4-carboxylic acidHCID 66643699—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(3-Isobutoxy-5-methyl-isoxazol-4-yl)-methanolHCID 6664358282.1%

Reaction Steps

To a stirred solution of 3-isobutoxy-5-methyl-isoxazole-4-carboxylic acid (146 mg, 0.73 mmol) and triethylamine (74 mg, 0.73 mmol) in tetrahydrofuran (5 mL) at −10° C. and under argon was added ethyl chloroformate (80 mg, 1.46 mmol). After 30 min, the mixture was filtered and the filter cake washed with tetrahydrofuran (4 mL). The combined filtrates were added to a solution of sodium borohydride (69 mg, 1.83 mmol) in water (2 mL) at 5° C. After 2 h the mixture was concentrated in vacuo, diluted with NaOH (2 N, 4 mL) then dried, filtered and concentrated in vacuo to give the title compound (111 mg, 82%) as a pale yellow oil. MS: m/e=186.3 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08357703B2
Source datasetuspto-grants-2013_01
ORD IDord-b09dd0b4508b4cb8925273028e508290
Source noteuspto-grants-2013_01