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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 262940Generated: October 31, 2026

Carbon Dioxide → N-Dodecyl-N-methylbenzenemethanamine

https://huagongshe.com/reaction/262940

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantFormic AcidHCID 284—
ReactantHydrochloric AcidHCID 313—
ReactantFormaldehydeHCID 712—
ReactantSodium HydroxideHCID 14798—
ReactantN-Benzyldodecan-1-amineHCID 232909—
SolventWaterHCID 962—
ProductN-Dodecyl-N-methylbenzenemethanamineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04155872
Source datasetuspto-grants-1979_05
ORD IDord-fb96d34ecf6347bb8636de81573ad3ee
Source noteuspto-grants-1979_05