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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 980532Generated: November 1, 2026

2-Aminobenzyl alcohol → HCID 13730769, compound

https://huagongshe.com/reaction/980532

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Aminobenzyl alcoholHCID 21439—
ReactantHCID 19352213HCID 19352213—
SolventEthanolHCID 702—
ProductHCID 13730769HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04638068
Source datasetuspto-grants-1987_01
ORD IDord-0c2209bff532473d827d5ceb079752d1
Source noteuspto-grants-1987_01