HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 262940Generated: October 31, 2026
Carbon Dioxide → N-Dodecyl-N-methylbenzenemethanamine
https://huagongshe.com/reaction/262940
Participants
| Role | Name | HCID | Charge |
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| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N-Benzyldodecan-1-amine | HCID 232909 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-Dodecyl-N-methylbenzenemethanamine | HCID 225125 | — |
Reaction Steps
To 8.96 g (0.105 mol.) of commercial formic acid (85~90%) which was cooled by cold water was gradually added 9.5 g (0.035 mol.) of N-benzyl-n-dodecylamine. Then 2.4 ml (0.0525 mol.) of formaldehyde (37%) was added to the mixture and heated at 90°~100° C. After several minutes, carbon dioxide gas generated, during which the mixture was cooled to room temperature. When the evolution of carbon dioxide stopped, the mixture was again refluxed at 90°~100° C. for 8 hours. After completing the reaction, 18 ml of 4 N-hydrochloric acid was added to the cooled reaction mixture, which was condensed to dryness under reduced pressure. The residue was dissolved in 5 ml of water. 10 ml of 18N-sodium hydroxide solution was added to the aqueous solution which was separated into an oily layer and an aqueous layer, the latter of which was extracted with benzene. The benzene extract was distilled under reduced pressure to obtain N-methyl-N-benzyl-n-dodecylamine, b.p. 146 ~ 149° C./0.4 mmHg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04155872 |
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| Source dataset | uspto-grants-1979_05 |
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| ORD ID | ord-fb96d34ecf6347bb8636de81573ad3ee |
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| Source note | uspto-grants-1979_05 |
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