HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 247768Generated: October 27, 2026
Hydrochloric Acid → 5-(N-acetylamino)-2-chloro-4-fluorophenylthioacetic acid
https://huagongshe.com/reaction/247768
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Thioglycolic Acid | HCID 1133 | — |
| Reactant | Sulfamic Acid | HCID 5987 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N-(5-amino-4-chloro-2-fluorophenyl)acetamide | HCID 11769584 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-(N-acetylamino)-2-chloro-4-fluorophenylthioacetic acid | HCID 178474230 | — |
Reaction Steps
4-(N-Acetylamino)-2-amino-1-chloro-5-fluorobenzene (7.0 g) was suspended in a mixture of conc. hydrochloric acid (9 ml), water (40 ml) and ice (60 g), and the suspension was kept at -5° to 10° C., preferably at 0° to 5° C. A solution of sodium nitrite (2.5 g) in water (8 ml) was dropwise added to the suspension, which was then stirred at the same temperature for 1 hour. To the thus prepared diazonium salt solution, sulfamic acid (0.2 g) was added, and the resultant mixture was added to a mixture of thioglycollic acid (4.1 g), basic cupric carbonate (2.3 g) and water (34 ml) and stirred at 15° to 25° C., followed by stirring for 30 minutes. A 50 % sodium hydroxide solution (8.4 ml) was dropwise added thereto to make pH at 7 to 8, followed by stirring at 95° to 100° C. for 1 hour. The reaction mixture was filtered by celite while hot to remove the copper salt. The filtrate was made acidic with conc. hydrochloric acid (12 ml) and extracted with ethyl acetate. The extract was dried, and the solvent was removed under reduced pressure to give 4.8 g of 5-(N-acetylamino)-2-chloro-4-fluorophenylthioacetic acid. M.P., 145.0°-147.0° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04709049 |
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| Source dataset | uspto-grants-1987_11 |
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| ORD ID | ord-8ce604013d9e426c89dbf2bfd04e9742 |
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| Source note | uspto-grants-1987_11 |
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