Carbofuran → HCID 20209289, compound

HRID 542145Notes

Reaction equation

HRID 542145 reaction equation
[CH3:1][C:2]1([CH3:16])[CH2:6][C:5]2[CH:7]=[CH:8][CH:9]=[C:10]([O:11][C:12]([NH:14][CH3:15])=[O:13])[C:4]=2[O:3]1.[CH3:17][O:18][P:19]([O:22]C)[O:20][CH3:21]>>[CH3:1][C:2]1([CH3:16])[CH2:6][C:5]2[CH:7]=[C:8]([P:19]([O:20][CH3:21])([O:18][CH3:17])=[O:22])[CH:9]=[C:10]([O:11][C:12]([NH:14][CH3:15])=[O:13])[C:4]=2[O:3]1

Participants

3

Reactant 2

HCID 2566CarbofuranHCID 8472Trimethyl phosphite

Product 1

HCID 20209289HCID 20209289, compoundYield 26%

Procedure

0.1 mole of carbofuran (2,3-dihydro-2,2-dimethyl-7-methylaminocarbonyloxybenzofuran) were reacted with trimethylphosphite analogously to Example 1a. The product was obtained in the form of an oil in a yield of 26%.

Workup

  1. customThe product was obtained in the form of an oil in a yield of 26%

Sources & evidence

ORD record
ord-68746eb5d1cc4aa98c220696f63d671e
Source dataset
uspto-grants-1987_04
Patent number
US04655883

Reaction notes

Loading…