HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 647246Generated: October 30, 2026
2-Chlorobenzoxazole → HCID 12763534, compound
https://huagongshe.com/reaction/647246
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chlorobenzoxazole | HCID 11986 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 12770729 | HCID 12770729 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 12763534 | HCID 12763534 | 94% |
Reaction Steps
First 20.5 g (0.1 mole) of hydroxyacetic acid N-isopropyl-N-(2-ethoxyethoxy)-amide and then 15.4 g (0.1 mole) of 2-chlorobenzoxazole were added dropwise to a solution of 6.2 g (0.11 mole) of potassium hydroxide in 200 ml of isopropanol at 0° to 5° C., and the mixture was then subsequently stirred for 6 hours, without cooling. The solvent was then distilled off in vacuo, the residue was dissolved in 200 ml of toluene and the solution was extracted by shaking once with 100 ml of water. The organic phase was dried over sodium sulphate and evaporated in vacuo. The residue was subjected to incipient distillation at 60° C. under a high vacuum. 30.3 g (94% of theory) of benzoxazol-2-yl-oxyacetic acid N-isopropyl-N-(2-ethoxy-ethoxy)-amide were obtained in this manner in the form of a light brown oil with a refractive index nD22 of 1.4986.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04408055 |
|---|
| Source dataset | uspto-grants-1983_10 |
|---|
| ORD ID | ord-6164323685534abc85173bac85603538 |
|---|
| Source note | uspto-grants-1983_10 |
|---|