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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 979495Generated: October 25, 2026

Hydrochloric Acid → HCID 68114514, compound

https://huagongshe.com/reaction/979495

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant(2,5-Dimethoxyphenyl)acetyl chlorideHCID 596088—
Reactant2-amino-5-(propan-2-yloxy)benzoic acidHCID 12719189—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
ProductHCID 68114514HCID 6811451475%

Reaction Steps

To a suspension of 9.8 g (50 mmol) of 5-isopropoxy-2-aminobenzoic acid and 11.0 g (80 mmol) of potassium carbonate in a mixed solvent of acetone (40 ml) and water (40 ml), 10.5 g (50 mmol) of 2,5-dimethoxyphenylacetic acid chloride were added dropwise at 10° C. After the resulting reaction mixture was stirred under ice cooling for 1 hour, stirring was continued for further 2 hours at room temperature. The thus obtained solution was made acidic with conc. hydrochloric acid and extracted with dichloromethane. After the extract was dried over magnesium sulfate, the solvent was distilled off to obtain 14.0 g (75%) of 2-(2,5-dimethoxyphenylacetylamino)-5-isopropoxybenzoic acid (m.p. 132°-135° C.). Then the thus obtained acid was heated under reflux for 2 hours in acetic anhydride (100 ml), followed by concentration under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluent: dichloromethane) to obtain 6.8 g of 2 -(2,5-dimethoxyphenylmethyl)-6-isopropoxy-4H-3,1-benzoxazine-4-one (yield from 5-isopropoxy-2-aminobenzoic acid: 36%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04668682
Source datasetuspto-grants-1987_05
ORD IDord-005146a8851e4f4fbb1576e5a874827b
Source noteuspto-grants-1987_05