Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methane | HCID 297 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 86757982 | HCID 86757982 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | HCID 86757983 | HCID 86757983 | 79.5% |
Reaction Steps
9 cm3 of distilled water are added to an oily suspension of 2.4 g of methyl 4-(N,N-di-n-propylaminomethylene)benzoate in 9 cm3 of concentrated hydrochloric acid (36% minimum), at a temperature close to 20° C. The reaction mixture is heated under reflux for 24 hours and then supplemented with 3S charcoal, and filtered while hot on a sintered glass. The filtrate is concentrated to dryness under reduced pressure (about 1 kPa) at a temperature close to 40° C. The white solid thus obtained is filtered on sintered glass, rinsed with 3 times 10 cm3 of acetonitrile, 10 cm3 of diisopropyl ether, air-dried and then dried under reduced pressure (about 0.2 kPa) at a temperature close to 50° C. 1.8 g of 4-(N,N-di-n-propylaminomethylene)benzoic acid (monohydrochloride) are thus obtained in the form of white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06380197B1 |
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| Source dataset | uspto-grants-2002_04 |
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| ORD ID | ord-0eddcec61eee4293985d19906bbc0eba |
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| Source note | uspto-grants-2002_04 |
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