HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl acetamido(4-bromo-2-nitrobenzyl)malonate → HCID 59627195, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl acetamido(4-bromo-2-nitrobenzyl)malonate | HCID 10622552 | — |
| Reactant | HCID 59627070 | HCID 59627070 | — |
| Reactant | HCID 59627186 | HCID 59627186 | — |
| Product | HCID 59627195 | HCID 59627195 | — |
Reaction Steps
Diethyl acetamido(5-chloro-3-methyl-2-nitrobenzyl)malonate (39) Following the procedure for the preparation of diethyl acetamido(4-bromo-2-nitrobenzyl)malonate (24) in Example 5,1-(bromomethyl)-5-chloro-3-methyl-2-nitrobenzene (38) was converted to the title product, which was obtained as a solid (65%). LCMS m/z 401.0 (M+1). 1H NMR (400 MHz, DMSO-d6) δ 1.15 (t, J=7.1 Hz, 6H), 1.90 (s, 3H), 2.24 (br s, 3H), 3.53 (s, 2H), 4.10-4.17 (m, 4H), 7.05 (br d, J=2.2 Hz, 1H), 7.56 (apparent dd, J=2.3, 0.7 Hz, 1H), 8.31 (br s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08183238B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-a00c580d85434550b904cfe1d30e688f |
| Source note | uspto-grants-2012_05 |