HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,5-Dimethoxybenzyl Bromide → 3-(3,5-Dimethoxybenzyl)-1-ethyl-5-methyl-2-oxoindolin-3-yl benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,5-Dimethoxybenzyl Bromide | HCID 1274490 | — |
| Reactant | 1-Ethyl-5-methyl-2-oxo-3-(3,4,5-trimethoxybenzyl)indolin-3-yl benzoate | HCID 86300681 | — |
| Reactant | 1-Ethyl-5-methyl-2-oxoindolin-3-yl benzoate | HCID 90415912 | — |
| Product | 3-(3,5-Dimethoxybenzyl)-1-ethyl-5-methyl-2-oxoindolin-3-yl benzoate | HCID 86301122 | — |
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 1-ethyl-5-methyl-2-oxoindolin-3-yl benzoate and 3,5-dimethoxy benzyl bromide (purchased from Fisher Scientific). 1H NMR δ 8.08 (d, 2H), 7.60 (t, 1H), 7.57 (t, 2H), 7.10 (d, 1H), 6.90 (s, 1H), 6.65 (d, 1H), 6.33 (s, 1H), 6.18 (s, 2H), 3.79 (m, 1H), 3.62 (s, 6H), 3.59 (m, 1H), 3.52 (d, 1H), 3.22 (d, 1H), 2.28 (s, 3H), 1.07 (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09079853B2 |
| Source dataset | uspto-grants-2015_07 |
| ORD ID | ord-3805f6d930f04e299e8e34610ffe3e27 |
| Source note | uspto-grants-2015_07 |