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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 723222Generated: October 31, 2026

Water → Methyl 4-[(5-aminopentyl)oxy]benzoate

https://huagongshe.com/reaction/723222

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHydrazineHCID 9321—
ReactantPotassium CarbonateHCID 11430—
Reactant4-[5-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-pentyloxy]-benzoic acid methyl esterHCID 57532228—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductMethyl 4-[(5-aminopentyl)oxy]benzoateHCID 5753222577%

Reaction Conditions

Temperature70 °C

Reaction Steps

A suspension of 4-[5-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-pentyloxy]-benzoic acid methyl ester (1 g, 2.72 mmol, Example 283: step a) and hydrazine (98.4 μL, 3.13 mmol) in MeOH:H2O (10 mL, 4:1) was heated to 65° C. for 2 hrs. Additional hydrazine was added (171 μL, 5.44 mmol) to the reaction mixture at rt. The reaction mixture was heated to 70° C. for 2 hrs then stirred overnight at rt. Potassium carbonate (30 mL, 1N aqueous) and methylene chloride (200 mL) were added to the reaction. The organic layer was dried over magnesium sulfate. The solvents were removed in vacuo to afford the title compound as a white solid (500 mg, 77%). 1H-NMR (CDCl3): δ 7.95–8.00 (m, 2H), 6.88–6.92 (m, 2H), 4.02 (t, 2H, J=6.43 Hz), 3.88 (s, 3H), 2.71–2.76 (m, 2H), 1.79–1.86 (m, 2H), 1.49–1.56 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07138530B2
Source datasetuspto-grants-2006_11
ORD IDord-f62e0e6e1c2a4c66b54ef3d7dbe78fab
Source noteuspto-grants-2006_11