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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1523097Generated: October 30, 2026

(2-Hydroxy-4-methoxybenzyl)-5-methyl-1-(4-methylpentyl)-2-oxoindolin-3-yl benzoate → 1-Ethyl-3-(2-hydroxy-5-methoxybenzyl)-5-methyl-2-oxoindolin-3-yl benzoate

https://huagongshe.com/reaction/1523097

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-Hydroxy-4-methoxybenzyl)-5-methyl-1-(4-methylpentyl)-2-oxoindolin-3-yl benzoateHCID 86301599—
Reactant1-Ethyl-5-methyl-2-oxoindolin-3-yl benzoateHCID 90415912—
Product1-Ethyl-3-(2-hydroxy-5-methoxybenzyl)-5-methyl-2-oxoindolin-3-yl benzoateHCID 86301597—

Reaction Steps

This compound was prepared in a similar manner to 3-(2-hydroxy-4-methoxybenzyl)-5-methyl-1-(4-methylpentyl)-2-oxoindolin-3-yl benzoate by reacting 1-ethyl-5-methyl-2-oxoindolin-3-yl benzoate with tert-butyl (2-(hydroxymethyl)-4-methoxyphenyl)carbonate. 1H-NMR δ 8.05 (d, 2H), 7.58 (t, 1H), 7.45 (t, 2H), 7.13 (m, 2H), 6.8 (d, 1H), 6.65 (m, 2H), 6.03 (d, 1H), 5.87 (bs, OH), 3.78 (m, 1H), 3.67 (d, 1H), 3.52 (m, 1H), 3.39 (s, 3H), 3.29 (d, 1H), 2.32 (s, 3H), 0.92 (t, 3H). Calculated mass for C26H25NO5 431.17. Observed 454.1 (M+Na).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09079853B2
Source datasetuspto-grants-2015_07
ORD IDord-071540905f0d482cb2babf48e5b45ac2
Source noteuspto-grants-2015_07