HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,4,5,6-Tetrahydrophthalic anhydride → Glyphosate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,4,5,6-Tetrahydrophthalic anhydride | HCID 12475 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Tartrazine | HCID 164825 | — |
| Reactant | Disodium tetrahydrophthalate | HCID 20290069 | — |
| Reactant | N-carboxymethyl-N-phosphonomethyl-3,4,5,6-tetrahydrophthalamic acid | HCID 20290081 | — |
| Product | Glyphosate | HCID 3496 | — |
| Product | Disodium | HCID 141233 | — |
Reaction Steps
The disodium salt of N-phosphonomethylglycine is prepared as described in Example III. The salt solution is stirred while 8.5 grams of 3,4,5,6-tetrahydrophthalic anhydride is added, along with sodium hydroxide to maintain the pH above 8. The reaction mixture is rotated overnight, after which a further 1.0 gram of anhydride is added and the reaction mixture stirred to completion. The mixture is filtered to yield a pink solution containing some disodium tetrahydrophthalate as a by-product. The reaction product is identified by nmr as the trisodium salt of N-carboxymethyl-N-phosphonomethyl-3,4,5,6-tetrahydrophthalamic acid. ##STR6##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04251257 |
| Source dataset | uspto-grants-1981_02 |
| ORD ID | ord-b64d81511d1742b6b025c13c3ff9111b |
| Source note | uspto-grants-1981_02 |