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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1870729Generated: November 1, 2026

Hydrochloric Acid → (2-Aminophenyl)(3-methoxyphenyl)methanone

https://huagongshe.com/reaction/1870729

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-Bromo-4-methoxyanilineHCID 10899671—
Reactant2-amino-N-methoxy-N-methylbenzamideHCID 11052242—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product(2-Aminophenyl)(3-methoxyphenyl)methanoneHCID 2213524274%

Reaction Conditions

Temperature-78 °C

Reaction Steps

In a flame-dried round bottom flask, anthranilic acid N-methoxyl-N-methylamide (8.00 g, 44.4 mmol) and m-bromoanisidine (8.31 g, 44.4 g) were dissolved in 250 mL of THF and the resulting solution was cooled to -78° C. With vigorous stirring, 2 equiv of nBuLi in hexanes (55.5 mL, 1.6 M, 88.8 mmol) was added dropwise by a syringe pump at 0.6 mL/min. After 20 min, 80 mL of 1 N hydrochloric acid was carefully added, the mixture was extracted with ethyl acetate (600 mL), and the ethyl acetate was washed with water (300 mL) and brine (300 mL), dried over sodium sulfate and concentrated in vacuo. Flash chromatography with 95:5 hexanes/ethyl acetate afforded 6.92 g (69% yield) of 2-amino-3'-methoxybenzophenone as a yellow oil. 2-Amino-3'-methoxybenzophenone was converted to 2-amino-3'-hydroxybenzophenone (below) prior to characterization.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06100254
Source datasetuspto-grants-2000_08
ORD IDord-9a8468b42af148ceb614fbf60629a576
Source noteuspto-grants-2000_08