HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminobenzyl alcohol → HCID 13730769, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminobenzyl alcohol | HCID 21439 | — |
| Reactant | HCID 19352213 | HCID 19352213 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 13730769 | HCID 13730769 | — |
Reaction Steps
To o-aminobenzyl alcohol, (2 g, 0.0125 mol) and 3-bromo-α-isopropyl-α-methyl-2,5-dioxo-3-pyrroline-1-acetonitrile (2.7 g, 0.01 mol) is added absolute ethanol (100 ml) containing 3 g of 5 A pulverized sieves. The mixture is stirred for 20 hours at room temperature. The solvent is removed and the residue is purified through a silica gel dry column, eluant ether-hexane (2:1). Starting bromomaleimide is first recovered, followed by a bright yellow solid 1.89 g (60%), mp 39°-45° C. Anal. calcd. for C17H19N3O3 : C, 65.16; H, 6.11; N, 13.41. Found: C, 65.94; H, 6.21; N, 12.87.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04638068 |
| Source dataset | uspto-grants-1987_01 |
| ORD ID | ord-0c2209bff532473d827d5ceb079752d1 |
| Source note | uspto-grants-1987_01 |