Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1811003Generated: November 1, 2026

Water → 2-(3-Bromo-2-methylphenyl)-6-methoxyisoindolin-1-one

https://huagongshe.com/reaction/1811003

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium t-butoxideHCID 23676156—
ReactantMethyl 2-((3-bromo-2-methylphenylamino)methyl)-5-methoxybenzoateHCID 66606189—
SolventTetrahydrofuranHCID 8028—
Product2-(3-Bromo-2-methylphenyl)-6-methoxyisoindolin-1-oneHCID 5937503475%

Reaction Steps

Step 3 A solution of methyl 2-((3-bromo-2-methylphenylamino)methyl)-5-methoxybenzoate (360 mg, 0.988 mmol) in THF (10 mL) was treated with sodium tert-butoxide (142 mg, 1.483 mmol) and stirred at rt overnight. The mixture was treated with water and extracted twice with DCM. The combined organic phases were washed with water, dried and concentrated. The residue was purified by column chromatography (eluting with EtOAc-hexane) to provide 2-(3-bromo-2-methylphenyl)-6-methoxyisoindolin-1-one as a white solid (246 mg, 75%). 1H NMR (400 MHz, chloroform-d) δ 7.62 (1 H, dd, J=7.9, 1.1 Hz), 7.46 (1 H, d, J=2.4 Hz), 7.42 (1 H, d, J=8.4 Hz), 7.15-7.26 (3 H, m), 4.67 (2 H, s), 3.92 (3 H, s), 2.34 (3 H, s). Mass spectrum m/z 332, 334 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362065B2
Source datasetuspto-grants-2013_01
ORD IDord-da3dbf8c450d4d1988d9fde8e7fe2bd0
Source noteuspto-grants-2013_01