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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1523095Generated: October 29, 2026

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

https://huagongshe.com/reaction/1523095

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-Hydroxy-4-methoxybenzyl)-5-methyl-1-(4-methylpentyl)-2-oxoindolin-3-yl benzoateHCID 86301599—
Reactant1-Ethyl-2-oxoindolin-3-yl benzoateHCID 90418154—
Product1-Ethyl-3-(2-hydroxy-4-methoxybenzyl)-2-oxoindolin-3-yl benzoateHCID 86301596—

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-2-oxoindolin-3-yl benzoate with tert-butyl (2-(hydroxymethyl)-5-methoxyphenyl)carbonate. 1H-NMR δ 8.04 (d, 2H), 7.6 (t, 1H), 7.43 (t, 2H), 7.30 (t, 1H), 7.25 (d, 1H), 7.08 (t, 1H), 6.78 (d, 1H), 6.47 (m, 2H), 6.24 (dd, 1H), 6.15 (bs, OH), 3.83 (m, 1H), 3.71 (s, 3H), 3.61 (m, 1H), 3.48 (d, 1H), 3.43 (d, 1H), 1.02 (t, 3H). Calculated mass for C25H23NO5, 417.16. Observed 440.0 (M+Na).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09079853B2
Source datasetuspto-grants-2015_07
ORD IDord-c74a807071d74d549d2e1a0c93f108b0
Source noteuspto-grants-2015_07