HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 273143Generated: October 26, 2026
Triethylamine → 1-[3-(3-Chloro-phenyl)-isoxazol-5-yl]-ethanol
https://huagongshe.com/reaction/273143
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Butyn-2-ol | HCID 16239 | — |
| Reactant | 3-Chloro-benzohydroximoyl chloride | HCID 72475911 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 1-[3-(3-Chloro-phenyl)-isoxazol-5-yl]-ethanol | HCID 67070766 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07456200B2 |
|---|
| Source dataset | uspto-grants-2008_11 |
|---|
| ORD ID | ord-fc1c58c04a2c403dacd0a0192753eb4f |
|---|
| Source note | uspto-grants-2008_11 |
|---|