HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 597669Generated: October 30, 2026
Hydrochloric Acid → HCID 86732895, compound
https://huagongshe.com/reaction/597669
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Phenol | HCID 996 | — |
| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Reactant | HCID 54253349 | HCID 54253349 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 86732895 | HCID 86732895 | — |
Reaction Steps
A mixture consisting of 21.9 g. (0.105 mole) phosphorus pentachloride, 150 ml. of carbon tetrachloride, and 25.83 g. (0.100 mole) o-(methylthio)benzoic acid 2-phenylhydrazide (prepared in Part A above) was heated at the reflux temperature until evolution of hydrogen chloride ceased. The reaction mixture was chilled in an ice-bath, and a suspension of 31.5 g, (0.335 mole) phenol in 50 ml. carbon tetrachloride was added. After removing the carbon tetrachloride by evaporation under reduced pressure, the resulting triphenylphosphate solution of the desired product was poured through a column of silica gel. Elution was effected with a mixture consisting of 1 part benzene and 1 part Skellysolve B. After removing the solvents from the eluate by evaporation under reduced pressure, 2.0 g. of residue was obtained. Recrystallization from petroleum ether gave an o-(methylthio)-chlorobenzoyl chloride phenylhydrazone having a melting point at 65° to 66.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04014932 |
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| Source dataset | uspto-grants-1977_03 |
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| ORD ID | ord-89d98ec38f514543aca7291010989af3 |
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| Source note | uspto-grants-1977_03 |
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