HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 251324Generated: October 25, 2026
Hydrochloric Acid → HCID 73554994, compound
https://huagongshe.com/reaction/251324
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2-((tert-Butoxycarbonyl)amino)-5-(trifluoromethyl)benzoic acid | HCID 15033886 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 73554994 | HCID 73554994 | — |
Reaction Steps
A suspension of 2-(tert-butoxycarbonylamino)-5-(trifluoromethyl)benzoic acid (56.34 g, 185 mmol, see: S. Takagishi, et al., Synlett 1992) in dioxane (100 mL) was treated with the dropwise addition of 4 N hydrochloric acid solution in dioxane (250 mL, 1.0 mol), and the mixture was stirred for 4 h. Analysis by LC/MS indicated that the reaction was not complete, so additional 4 N hydrochloric acid solution in dioxane (250 mL, 1.0 mol) was added, and the mixture was stirred overnight. Analysis by LC/MS indicated that the reaction still contained c. 5% of the starting material, so additional 4 N hydrochloric acid solution in dioxane (100 mL, 0.4 mol) was added, and the mixture was stirred for 4 h. Analysis by LC/MS indicated that the reaction was now complete. The mixture was concentrated in-vacuo, and the residue was stripped 2× from methylene chloride to remove any remaining HCl. The 2-amino-5-(trifluoromethyl)benzoic acid, hydrochloride thus obtained was used immediately in the next step. MS (ES+)=206 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07863333B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-39f0bcf8bea74444802e54e2a70ea048 |
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| Source note | uspto-grants-2011_01 |
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