HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156421Generated: October 28, 2026
3,4-Dichlorobenzotrifluoride → HCID 13094093, compound
https://huagongshe.com/reaction/1156421
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,4-Dichlorobenzotrifluoride | HCID 9481 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Reactant | 2-[2-[[2-(2,5-Dihydroxyphenyl)phenyl]methoxymethyl]phenyl]benzene-1,4-diol | HCID 131711022 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 13094093 | HCID 13094093 | 70% |
Reaction Steps
To as flask equipped with a stirrer, thermometer, condenser and drying tube are charged 3,4-dichlorobenzotrifluoride (43 g., 0.20 mole), potassium 4-benzyloxyphenate (47.5 g., 0.20 mole-prepared from hydroquinone monobenzylether using potassium hydroxide pellets dissolved in methanol and removal of the solvent in vacuo and subsequent precipitation in ether) and dimethyl sulfoxide (400 ml.). The reaction mixture is then warmed to 120° C. and maintained at 135° C. for 3 hours, cooled, poured into water (3 liters) and extracted into hexane (500 ml., then 300 ml., then 200 ml.) and the combined hexane extracts washed again with water (200 ml.), dried with anhydrous magnesium sulfate, and the solvent removed in vacuo to give 52.6 g. (70% yield) of 4-benzyloxyphenyl 2-chloro-4-trifluoromethylphenyl ether, mp 63°-6° C., which is recrystallized from methanol to give white crystals, mp 69°-71° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04335249 |
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| Source dataset | uspto-grants-1982_06 |
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| ORD ID | ord-dfce760f351d463eb56e6c1b34498f2d |
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| Source note | uspto-grants-1982_06 |
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