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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1955256Generated: November 1, 2026

Triethylamine → 5-(2-Benzyloxy-ethoxy)-1,3-dihydro-indol-2-one

https://huagongshe.com/reaction/1955256

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant[5-(2-Benzyloxy-ethoxy)-2-nitro-phenyl]-acetic acidHCID 23294499—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
Product5-(2-Benzyloxy-ethoxy)-1,3-dihydro-indol-2-oneHCID 2329427979%

Reaction Steps

A mixture of [5-(2-benzyloxy-ethoxy)-2-nitro-phenyl]-acetic acid (0.58 g, 1751 mmol), 5% palladium on carbon (0.05 g) and triethylamine (0.37 ml, 2.66 mmol) in methanol (35 ml) was stirred under a hydrogen atmosphere (1 atm) for 3 h. After removal of the catalyst by filtration, the filtrate was evaporated to give a yellow oil. The oil was dissolved in 10 ml of acetic acid and the solution was stirred at 80° C. under argon for 3 h. The acetic acid was removed on a rotavap. The residue was dissolved in a small amount of methylene chloride and chromatographed on silica gel eluted with 30% ethyl acetate in methylene chloride to give 5-(2-benzyloxy-ethoxy)-1,3-dihydro-indol-2-one (0.39 g, 79%) as a white solid. Analysis calculated for C17H17NO3 : C, 72.07; H, 6.05; N, 4.85. Found: C, 72.09; H, 6.01; N, 4.85.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06124323
Source datasetuspto-grants-2000_09
ORD IDord-14e74948d82949caa0ec653cfef2aa52
Source noteuspto-grants-2000_09