HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 5-Benzoxazoleacetic acid, 2-(4-chlorophenyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methyl alpha-bromo-2-p-chlorophenyl-5-benzoxazolylacetate | HCID 53740102 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 5-Benzoxazoleacetic acid, 2-(4-chlorophenyl)- | HCID 3039778 | — |
Reaction Steps
A solution of methyl α-bromo-2-p-chlorophenyl-5-benzoxazolylacetate (3 g.) in dioxan (30 ml.) was treated with aqueous 2N sodium hydroxide solution. The mixture was acidified and crude α-bromo-2-p-chlorophenyl-5-benzoxazolylacetic acid was filtered off. This solid was dissolved in ethanol (30 ml.) and palladium on charcoal added. The solution was hydrogenated for 3 hours. The catalyst was removed and the solution was evaporated to dryness. The residue was crystallised to give 2-p-chlorophenyl-5-benzoxazolylacetic acid, m.p. 241°-242° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04025636 |
| Source dataset | uspto-grants-1977_05 |
| ORD ID | ord-ef576e6f8a8e4fbeb47d5cbf4a4f4bf3 |
| Source note | uspto-grants-1977_05 |