HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1717458Generated: October 27, 2026
Sulfuryl chloride → 2-Amino-3-chloro-5-(trifluoromethoxy)benzoic acid
https://huagongshe.com/reaction/1717458
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | 2-amino-5-(trifluoromethoxy)benzoic Acid | HCID 11085349 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-Amino-3-chloro-5-(trifluoromethoxy)benzoic acid | HCID 21904619 | 107.6% |
Reaction Steps
To a solution of 2-amino-5-trifluoromethoxybenzoic acid (49.0 g, 0.22 mol; see step (ii) above) in HOAc (1200 mL) was slowly added sulfuryl chloride (41.8 g, 0.31 mol). Gas evolution was observed. The resulting heterogeneous mixture was stirred at room temperature for 1 h. Additional HOAc (300 mL) was added to aid stirring, followed by sulfuryl chloride in 5 mL portions until the starting material was consumed based on TLC analysis. The reaction was concentrated in vacuo to give solids that were flushed on a rotary evaporator with EtOAc (2×) followed by Et2O (1×) to remove the HOAc. The resulting solids were further dried to give the HCl salt of the crude sub-title compound (60.5 g, 94%), which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07803954B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-279001468c854fc0bdf3487386f5874f |
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| Source note | uspto-grants-2010_09 |
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