Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Quinisocaine | HCID 6857 | — |
| Reactant | Barium Sulfate | HCID 24414 | — |
| Reactant | Sulfur | HCID 5362487 | — |
| Reactant | HCID 20534493 | HCID 20534493 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 20534474 | HCID 20534474 | 62.7% |
Reaction Steps
A mixture of 43.92 g of 2-methyl-3-(p-chlorobenzoyl)-benzoic acid chloride, 450 ml of xylene, 4.5 g of barium sulfate containing 10% palladium and 0.4 ml of a solution obtaining by refluxing 6 g of quinolein and 1 g of sulfur for 5 hours was cooled and then was diluted with 70 ml of xylene. The mixture was stirred at 130° C. while passing hydrogen therethrough for 45 minutes and the said temperature was held until evolution of hydrochloric acid ceased. An inert gas was passed therethrough at 130° C. and the mixture was then cooled to 30° C. and filtered to remove the catalyst. The solvent was distilled off and the residual oil was dissolved in isopropyl ether. Sodium bisulfite was added to the resulting solution and the mixture was stirred for 18 hours. The bisulfitic compound which precipitated was recovered by vacuum filtration, was washed and was then decomposed by stirring for 21/2 hours in the presence of dilute sulfuric acid and ether under an inert gas. The ether was decanted and the aqueous phase was extracted with ether. The combined ether phases were washed with water, dried and evaporated to dryness under reduced pressure. The residue was crystallized from isopropyl ether to obtain 24.3 g of 2-methyl-3-(p-chlorobenzoyl)-benzaldehyde melting at 68° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04027040 |
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| Source dataset | uspto-grants-1977_05 |
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| ORD ID | ord-f7f8140bfbeb4d1d9286d54d7fce860d |
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| Source note | uspto-grants-1977_05 |
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