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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2104140Generated: October 30, 2026

3,5-Heptanedione → HCID 11523520, compound

https://huagongshe.com/reaction/2104140

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-HeptanedioneHCID 81923—
Reactant2-Amino-5-bromobenzophenoneHCID 99677—
ReactantSodiumHCID 5360545—
SolventEthanolHCID 702—
ProductHCID 11523520HCID 1152352037%

Reaction Steps

The title compound was prepared according to the general procedure of method A. The (2-Amino-5-bromo-phenyl)-phenyl-methanone [example A16] (on 0.1-1 g scale) and 3,5-heptanedione (1.5 equiv) and sodium tetrachloroaureate(III) dihydrate (0.025 equiv) were heated in parallel in a Radley carousel under nitrogen in ethanol (10% w/w-solution of (2-Amino-5-bromo-phenyl)-phenyl-methanone) and reacted for 24 h. The reaction mixture was evaporated to dryness and the residue purified by chromatography on silica gel in heptane/ethyl acetate (20:1). Yield: 37%. MS: m/z=368 (M).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576217B2
Source datasetuspto-grants-2009_08
ORD IDord-25fab1815f5e4638b226261b45007917
Source noteuspto-grants-2009_08