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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1397260Generated: November 2, 2026

HCID 86677590, compound → HCID 67323924, compound

https://huagongshe.com/reaction/1397260

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86677590HCID 86677590—
ReactantHCID 178418332HCID 178418332—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67323924HCID 6732392449%

Reaction Conditions

Temperature0 °C

Reaction Steps

The compound methyl 3-bromo-5-(methoxy(methyl)carbamoyl)benzoate (2.3 g, 7.6 mmol) was dissolved in dry THF (50 mL), solution was cooled to 0° C. and methylmagnesium chloride (3M in THF, 2.5 mL, 7.6 mmol)) was added dropwise. The reaction mixture was slowly allowed to come to room temperature and stirred further for 6 h. The reaction mixture was cooled to 0° C. and quenched with saturated NH4Cl solution. The product was extracted with EtOAc. The organic layer was washed with water and brine and dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure. The crude product was purified by column chromatography (silica 60-120 mesh, eluent 5% EtOAc in petroleum ether) to get methyl 3-acetyl-5-bromobenzoate (0.95 g, yield 49%) as a white solid. 1H NMR (400 MHz, CDCl3) δ 8.51 (t, J=1.3 Hz, 1H), 8.37 (t, J=1.7 Hz, 1H), 8.28 (t, J=1.6 Hz, 1H), 3.97 (s, 3H), 2.65 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901156B2
Source datasetuspto-grants-2014_12
ORD IDord-2b36207596484506a5cedc1dacfb55c5
Source noteuspto-grants-2014_12