HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358184Generated: October 30, 2026
2-Chlorobenzoxazole → HCID 13090853, compound
https://huagongshe.com/reaction/358184
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Chlorobenzoxazole | HCID 11986 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | N-(2,2,2-trifluoroethyl)-N-methyl-hydroxyacetic acid amide | HCID 13090851 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 13090853 | HCID 13090853 | 52% |
Reaction Steps
17.1 g (0.1 mol) of N-(2,2,2-trifluoroethyl)-N-methyl-hydroxyacetic acid amide and 7 g of potassium hydroxide powder were initially introduced into 100 ml of acetonitrile at 20° C., and 15.3 g (0.1 mol) of 2-chlorobenzoxazole were added at a temperature between 20° and 40° C. The reaction mixture was stirred at 40° C. for one hour and at 20° C. for a further 15 hours and was concentrated and the concentrate was shaken with toluene and water. The organic phase was washed with dilute sodium hydroxide solution, washed until neutral, dried and filtered. The solvent was carefully distilled off from the filtrate under reduced pressure. 15 g (52% of theory) of N-(2,2,2-trifluoroethyl)-N-methyl-benzoxazol-2-yl-oxy-acetic acid amide of melting point 92° C. were obtained as the residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04465504 |
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| Source dataset | uspto-grants-1984_08 |
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| ORD ID | ord-1a97c3c698a64f23bf2f33a17833901d |
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| Source note | uspto-grants-1984_08 |
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