Acetic Acid → 7-Azido-2-[(4-nitrophenyl)methylene]-3-oxoheptanoic acid 2-cyanoethyl ester

HRID 396683Notes

Reaction equation

HRID 396683 reaction equation
[N:1]([CH2:4][CH2:5][CH2:6][CH2:7][C:8]([CH:10]1[C:15](=[O:16])[O:14][C:13]([CH3:18])(C)O[C:11]1=O)=[O:9])=[N+:2]=[N-:3].OCC[C:23]#[N:24].C(=O)=O.[N+:28]([C:31]1[CH:38]=[CH:37][C:34](C=O)=[CH:33][CH:32]=1)([O-:30])=[O:29].N1CCCCC1.C(O)(=O)C>CC(O)C.CCOC(C)=O.CCCCCC>[C:23]([CH2:18][CH2:13][O:14][C:15](=[O:16])[C:10](=[CH:11][C:34]1[CH:37]=[CH:38][C:31]([N+:28]([O-:30])=[O:29])=[CH:32][CH:33]=1)[C:8](=[O:9])[CH2:7][CH2:6][CH2:5][CH2:4][N:1]=[N+:2]=[N-:3])#[N:24]

Participants

10

Procedure

5-(5-Azidopentanoyl)-2,2-dimethyl-1,3-dioxane-4,6-dione was heated with 3-hydroxypropionitrile (2.42 g, 34.0 mmol) at 80° C. until no more CO2 was released. After cooling to room temperature, the mixture was diluted with 150 ml of 2-propanol, and 4-nitrobenzaldehyde (4.60 g, 30.3 mmol), piperidine (130 mg, 1.50 mmol) and acetic acid (90 mg, 1.50 mmol) were added. The mixture was stirred at room temperature for 48 hrs. The product, 7-azido-2-[(4-nitrophenyl)methylene]-3-oxoheptanoic acid 2-cyanoethyl ester was obtained as a pale-yellow oil (5.73 g, 51% yield) after chromatography (SiO2, Hexane: AcOEt, 2:1).

Workup

  1. additionwere added

Sources & evidence

ORD record
ord-22348eeacdec4d7eb44edcc06f555659
Source dataset
uspto-grants-2003_08
Patent number
US06608086B2

Reaction notes

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