Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 3-Amino-4-chlorobenzoic acid | HCID 76092 | — |
| Reactant | Potassium ethylxanthate | HCID 2735045 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Catalyst | Nickel Dichloride | HCID 24385 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 13139571 | HCID 13139571 | — |
Reaction Steps
3-Amino-4-chlorobenzoic acid (34.3g) was added to 5N hydrochloric acid (120 ml) and cooled to 0° C. To the stirred suspension was added a solution of sodium nitrite (14.5g) in water (35 ml) over 30 min. with the temperature maintained at 0° to 5° C. The yellow diazonium solution, containing some suspended solid was added to a solution of potassium ethyl xanthate (37.5g) in water (60 ml), containing 0.2g nickel chloride, at 45°-50° C. Nitrogen evolution occurred and the yellow solid which precipitated at first decomposed to a red oil which then solidified. When the addition was complete, the mixture was heated to 70° C., cooled, and the red solid filtered off and washed with water. It was then boiled with a solution of potassium hydroxide (60 g) in water (300 ml) for 2 hr., cooled, filtered and acidified with excess hydrochloric acid. Thin-layer chromatography indicated the presence of 2 components in the precipitated creamy solid. Recrystallisation from acetic acid yielded a by-product, m.p. 240°-290° C., and dilution of the recrystallisation liquors gave a solid which was recrystallised from aqueous ethanol yielding mainly 4-chloro-3-mercapto-benzoic acid, m.p. 209°-211° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04025635 |
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| Source dataset | uspto-grants-1977_05 |
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| ORD ID | ord-d1bccde971f548989bbfa04fc3c4d2d9 |
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| Source note | uspto-grants-1977_05 |
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