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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 732055Generated: October 26, 2026

Triethylamine → 1-[3-(3-Chloro-phenyl)-isoxazol-5-yl]-ethanol

https://huagongshe.com/reaction/732055

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-Butyn-2-olHCID 16239—
Reactant3-Chloro-benzohydroximoyl chlorideHCID 72475911—
SolventBenzeneHCID 241—
SolventHydrochloric AcidHCID 313—
Product1-[3-(3-Chloro-phenyl)-isoxazol-5-yl]-ethanolHCID 67070766—

Reaction Conditions

Temperature0 °C

Reaction Steps

3-Chloro-benzohydroximoyl chloride (e.g. Kim, Jae Nyoung; Ryu, Eung K; J. Org. Chem. (1992), 57(24), 6649-50) (2.84 g, 14.8 mmol) was suspended in benzene (50 ml) and cooled to 0° C. 3-Butyn-2-ol (2.10 g, 29.9 mmol) and triethylamine (1.89 ml, 26.7 mmol) were added. The mixture was heated to 60° C. for 1.5 houes, cooled and diluted with benzene and 1N aqueous hydrochloric acid. After stirring, the separated benzene layer was evaporated to dryness and the crude purified via flash chromatography over silica using heptane/ethyl acetate=5/1 giving after drying in vacuo the title compound (0.49 g, 15%). 1H NMR (CDCl3), δ (ppm): 1.64 (d, 3 H), 5.07 (dq, 1 H), 6.50 (s, 1 H), 7.40 (m, 2 H), 7.68 (m, 1 H), 7.79 (m, 1 H),

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07585881B2
Source datasetuspto-grants-2009_09
ORD IDord-f6dc243d6b7b468d8f740a9b7c9f0fff
Source noteuspto-grants-2009_09