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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 323838Generated: October 27, 2026

Hydrochloric Acid → Benzenethiol, 2-amino-3,4,6-trifluoro-, hydrochloride

https://huagongshe.com/reaction/323838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,4-DioxaneHCID 31275—
Reactant4,5,7-Trifluoro-2-methylbenzothiazoleHCID 10375600—
SolventEthylene GlycolHCID 174—
SolventSodium HydroxideHCID 14798—
ProductBenzenethiol, 2-amino-3,4,6-trifluoro-, hydrochlorideHCID 1139028273%

Reaction Conditions

Temperature125 °C

Reaction Steps

A solution of 4,5,7-trifluoro-2-methylbenzothiazole (25.0 g, 123 mmol) in ethylene glycol (310 mL, 0.4 M) and 30% aq. NaOH (310 mL, 0.4 M) was degassed using a nitrogen stream then heated to a gentle reflux (125° C.) for 3 h. The solution was cooled to 0° C. and acidified to pH 3-4 using conc. HCl (appox. 200 mL). The solution was extracted with ether (750 mL) and washed with water (200 mL). The organic layer was dried over Na2SO4, filtered and treated with 2,2-di-tert-butyl-4-methylphenol (0.135 g, 0.5 mol %). After concentrating to dryness, the crude product was dissolved in anhydrous methanol (200 mL) and treated with an HCl solution in 1,4-dioxane (37 mL, 4 N, 148 mmol). The resulting mixture was concentrated to dryness, triturated with isopropylether (100 mL) and filtered to give 2-amino-3,4,6-trifluorothiophenol hydrochloride (19.3 g, 73%) as a light brown solid that was used without further purification. mp. 121-124° C.; Rf 0.43 (30% ethyl acetate in heptane); Anal. Calcd for C6H5ClF3NS: C, 33.42; H, 2.34; N, 6.50; S, 14.87. Found C, 33.45; H, 2.27; N, 6.48; S, 14.96.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06214991B1
Source datasetuspto-grants-2001_04
ORD IDord-ac26499faf8a41d0aa002fa76ae70ca7
Source noteuspto-grants-2001_04