Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | N-Methylaniline | HCID 7515 | — |
| Reactant | HCID 86736350 | HCID 86736350 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-Methylformanilide | HCID 66737 | — |
Reaction Steps
To the reactor described in Example 1 is charged 107 grams (1.0 mole) of N-methyl aniline, 14 grams (0.1 mole) of sodium formanilide and 150 milliliters of methanol. The autoclave is closed, purged with carbon monoxide and the temperature raised to 100° C. with atmospheric steam. Carbon monoxide is then introduced at 28 kg/cm2 pressure for about 30 minutes. The basic reaction mixture is neutralized with hydrochloric acid and extracted with xylene. Gas liquid chromatographic analysis shows that a high conversion to N-methyl formanilide is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04140716 |
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| Source dataset | uspto-grants-1979_02 |
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| ORD ID | ord-d262158082704a289cdfb604fdffea36 |
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| Source note | uspto-grants-1979_02 |
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