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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantThioglycolic AcidHCID 1133—
ReactantSulfamic AcidHCID 5987—
ReactantSodium HydroxideHCID 14798—
ReactantN-(5-amino-4-chloro-2-fluorophenyl)acetamideHCID 11769584—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
Product5-(N-acetylamino)-2-chloro-4-fluorophenylthioacetic acidHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04709049
Source datasetuspto-grants-1987_11
ORD IDord-8ce604013d9e426c89dbf2bfd04e9742
Source noteuspto-grants-1987_11