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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2-Bromo-4-methoxyaniline | HCID 10899671 | — |
| Reactant | 2-amino-N-methoxy-N-methylbenzamide | HCID 11052242 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2-Aminophenyl)(3-methoxyphenyl)methanone | HCID 22135242 | 74% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06100254 |
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| Source dataset | uspto-grants-2000_08 |
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| ORD ID | ord-9a8468b42af148ceb614fbf60629a576 |
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| Source note | uspto-grants-2000_08 |
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