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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707278Generated: November 2, 2026

tert-Butyl 3-aminocrotonate → HCID 18962946, compound

https://huagongshe.com/reaction/1707278

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 3-aminocrotonateHCID 12221517—
Reactant8-Chloro-3-[(2,3-dichlorophenyl)methylidene]octane-2,4-dioneHCID 54257843—
Solvent1-ButanolHCID 263—
ProductHCID 18962946HCID 18962946—

Reaction Steps

25 g (70 mmol) 6-(2,3-dichlorophenyl-methylene)-1-chloro-5,7-octanedione and 22 g (0.14 mol) tert-butyl β-amino-crotonate are boiled under reflux in 200 ml 1-butanol for 6 h. The mixture is concentrated and the residue is prepurified by chromatography with toluene/acetone=8/2. The product thus obtained is chromatographed again over silica gel with toluene/acetone=99/1. The title compound is obtained as a yellow oil. Yield: 5.8 g (18%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05352684
Source datasetuspto-grants-1994_10
ORD IDord-6338a497ca4b481481c47ffc06471a26
Source noteuspto-grants-1994_10