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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1523090Generated: October 30, 2026

3,4-Dimethoxybenzyl bromide → 3-(3,4-Dimethoxybenzyl)-5-methyl-2-oxo-1-propylindolin-3-yl benzoate

https://huagongshe.com/reaction/1523090

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-Dimethoxybenzyl bromideHCID 10900458—
Reactant1-Ethyl-5-methyl-2-oxo-3-(3,4,5-trimethoxybenzyl)indolin-3-yl benzoateHCID 86300681—
Reactant5-Methyl-2-oxo-1-propylindolin-3-yl benzoateHCID 90417475—
Product3-(3,4-Dimethoxybenzyl)-5-methyl-2-oxo-1-propylindolin-3-yl benzoateHCID 86300970—

Reaction Steps

This compound was made in an analogous fashion to 1-ethyl-5-methyl-2-oxo-3-(3,4,5-trimethoxybenzyl)indolin-3-yl benzoate using 5-methyl-2-oxo-1-propylindolin-3-yl benzoate and 4-(bromomethyl)-1,2-dimethoxybenzene. 1H-NMR δ 8.06 (d, 2H), 7.57 (t, 1H), 7.43 (t, 2H), 7.07 (d, 1H), 6.90 (s, 1H), 6.68 (d, 1H) 6.62 (m, 2H), 6.39 (s, 1H), 3.83 (s, 3H), 3.66 (s, 3H), 3.56 (m, 1H) 3.47 (m, 2H), 3.25 (d, 1H), 2.27 (s, 3H), 1.52 (m, 2H), 0.84 (t, 3H). Calculated mass for C28H29NO5, 459.53. Observed 482.2 (M+Na).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09079853B2
Source datasetuspto-grants-2015_07
ORD IDord-2a6fff07cf8242b8a1d5f05f94c1719a
Source noteuspto-grants-2015_07