Pyrimethanil → HCID 86755179, compound

HRID 378247Notes

Reaction equation

HRID 378247 reaction equation
[CH3:1][C:2]1[CH:3]=[C:4]([CH3:15])[N:5]=[C:6]([NH:8][C:9]2[CH:10]=[CH:11][CH:12]=[CH:13][CH:14]=2)[N:7]=1.[C:16]([OH:35])(=[O:34])[CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23]/[CH:24]=[CH:25]\[CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH3:33]>C1(C)C=CC=CC=1>[CH3:1][C:2]1[CH:3]=[C:4]([CH3:15])[N:5]=[C:6]([NH:8][C:9]2[CH:10]=[CH:11][CH:12]=[CH:13][CH:14]=2)[N:7]=1.[C:16]([O-:35])(=[O:34])[CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23]/[CH:24]=[CH:25]\[CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH3:33]

Participants

4

Reactant 2

HCID 91650PyrimethanilHCID 445639Oleic Acid

Product 1

HCID 86755179HCID 86755179, compound

Reagents, catalysts & solvents 1

HCID 1140TolueneSolvent

Procedure

A solution of pyrimethanil (1.0 g), toluene (50 ml) and oleic acid (1.42 g) was allowed to stand overnight at room temperature. The toluene was evaporated under reduced pressure to give pyrimethanil oleate, as an oil. (compound 1) nmr data:

Workup

  1. customThe toluene was evaporated under reduced pressure

Sources & evidence

ORD record
ord-249ab6c240054591a095b4d67b713e79
Source dataset
uspto-grants-2000_02
Patent number
US06030977

Reaction notes

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