Glyphosate → Glyphosate

HRID 2049231Notes

Reaction equation

HRID 2049231 reaction equation
C1(=O)OC(=O)C=C1.[OH-].[Na+:9].[P:10]([CH2:14][NH:15][CH2:16][C:17]([OH:19])=[O:18])([OH:13])([OH:12])=[O:11].C1C(N=NC2C(=O)N(C3C=CC(S([O-])(=O)=O)=CC=3)N=C2C([O-])=O)=CC=C(S([O-])(=O)=O)C=1.[Na+:51].[Na+].[Na+].C(CN(CP(O)(O)=O)C(=O)/C=C\C(O)=O)(O)=O>CCOCC>[Na:9][Na:51].[P:10]([CH2:14][NH:15][CH2:16][C:17]([OH:19])=[O:18])([OH:13])([OH:12])=[O:11]

Participants

8

Procedure

A solution of the disodium salt of N-phosphonomethylglycine is prepared as described in Example I and 11.0 grams (0.11 mole) of finely ground maleic anhydride is added with stirring. Some sodium hydroxide is added to keep the pH at almost 9, and a small portion of ether is added to help dissolve particles of the anhydride. Stirring is continued for several days, and 2.0 or 4.0 gram portions of maleic anhydride are added until no further N-phosphonomethylglycine remains in the reaction mixture. During this period, small portions of sodium hydroxide are added as needed to maintain a pH of about 8. When reaction is complete, the mixture is filtered, rinsed with water, concentrated and then dried. The product, containing disodium maleate by-product, is obtained as a colorless glass, and it is identified by nuclear magnetic resonance (nmr) as the trisodium salt of N-carboxymethyl-N-(phosphonomethyl)maleamic acid. ##STR4##

Workup

  1. additionis added
  2. stirringStirring
  3. waitis continued for several days
  4. waitDuring this period
  5. temperatureto maintain a pH of about 8
  6. customWhen reaction
  7. filtrationthe mixture is filtered
  8. washrinsed with water
  9. concentrationconcentrated
  10. customdried
  11. additionThe product, containing disodium maleate by-product
  12. customis obtained as a colorless glass, and it

Sources & evidence

ORD record
ord-6ee2bec660364fa6b452b2c3065a2a6d
Source dataset
uspto-grants-1980_04
Patent number
US04197254

Reaction notes

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