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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuryl chlorideHCID 24648—
Reactant2-amino-5-(trifluoromethoxy)benzoic AcidHCID 11085349—
SolventAcetic AcidHCID 176—
Product2-Amino-3-chloro-5-(trifluoromethoxy)benzoic acidHCID 21904619107.6%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803954B2
Source datasetuspto-grants-2010_09
ORD IDord-279001468c854fc0bdf3487386f5874f
Source noteuspto-grants-2010_09