HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pentabromophenol → o-(Pentabromphenoxymethyl)-benzoic acid-(pentabromophenyl) ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pentabromophenol | HCID 11852 | — |
| Reactant | Phenolate | HCID 119047 | — |
| Reactant | Pentabromophenyl 2-(chloromethyl)benzoate | HCID 20314961 | — |
| Solvent | 2-Methoxyethanol | HCID 8019 | — |
| Solvent | Potassium Hydroxide | HCID 14797 | — |
| Product | o-(Pentabromphenoxymethyl)-benzoic acid-(pentabromophenyl) ester | HCID 53683769 | — |
Reaction Steps
In a two-liter flask, 5.6 of potassium hydroxide was dissolved at 75° C in 800 ml of methyl glycol; then 48.9 g (= 0.1 mole) of pentabromphenol was stirred in. To this phenolate solution, at 75° C, 64.15 g was added of the o-chloromethylbenzoic acid pentabromophenyl ester, prepared as in Example 9a, and the mixture was heated with stirring to ebullition. It was refluxed for an hour, then cooled, and the solids were isolated and worked up as described in the preceding examples.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04105628 |
| Source dataset | uspto-grants-1978_08 |
| ORD ID | ord-5273b953593440aa9322852122727cdb |
| Source note | uspto-grants-1978_08 |