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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2222774Generated: October 27, 2026

Acetyl chloride → 2-Ethanoyloxy-5-tert-butoxycarbonylaminobenzoic acid

https://huagongshe.com/reaction/2222774

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantPotassium CarbonateHCID 11430—
Reactant5-(N-tert-Butoxycarbonylamino)salicylic AcidHCID 10377562—
SolventDimethylformamideHCID 6228—
Product2-Ethanoyloxy-5-tert-butoxycarbonylaminobenzoic acidHCID 2234190152.2%

Reaction Steps

To a solution of 5-tert-butoxycarbonylamino-2-hydroxybenzoic acid (1.02 g, 4.02 mmole) in DMF (20.0 ml) was added with acetyl chloride (39 mg, 4.83 mmole) and potassium carbonate (555 mg, 4.02 mmole). The reaction mixture was stirred for 4 hr at room temperature. After the reaction mixture was concentrated, the residue was dissolved in ethyl acetate. The organic layer was washed with water and brine and dried over anhydrous Na2SO4. After evaporation of the solvent, the residue was recrystallized from ethyl acetate/hexane to give 0.62 g (52% yield) of 2-ethanoyloxy-5-tert-butoxycarbonylaminobenzoic acid as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07371896B2
Source datasetuspto-grants-2008_05
ORD IDord-c57644a3b40c4503868f5f0e5937bf18
Source noteuspto-grants-2008_05