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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 647246Generated: October 30, 2026

2-Chlorobenzoxazole → HCID 12763534, compound

https://huagongshe.com/reaction/647246

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorobenzoxazoleHCID 11986—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 12770729HCID 12770729—
SolventIsopropanolHCID 3776—
ProductHCID 12763534HCID 1276353494%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04408055
Source datasetuspto-grants-1983_10
ORD IDord-6164323685534abc85173bac85603538
Source noteuspto-grants-1983_10