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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1163858Generated: October 25, 2026

N,N-Dimethyl-1,3-propanediamine → 9-((3Z)-Non-3-en-1-yl)-10-octylnonadecanedioic acid

https://huagongshe.com/reaction/1163858

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-Dimethyl-1,3-propanediamineHCID 7993—
Reactant(3E,5E,7E,9E,11E,13E,15E,17E)-18-[(3E,5E,7E,9E,11E,13E,15E,17E)-18-[(3E,5E,7E,9E,11E,13E,15E)-octadeca-3,5,7,9,11,13,15,17-octaenoyl]oxyoctadeca-3,5,7,9,11,13,15,17-octaenoyl]oxyoctadeca-3,5,7,9,11,13,15,17-octaenoic acidHCID 6437702—
SolventO-XyleneHCID 7237—
Product(3E,5E,7E,9E,11E,13E,15E,17E)-18-[(3E,5E,7E,9E,11E,13E,15E,17E)-18-[(3E,5E,7E,9E,11E,13E,15E)-octadeca-3,5,7,9,11,13,15,17-octaenoyl]oxyoctadeca-3,5,7,9,11,13,15,17-octaenoyl]oxyoctadeca-3,5,7,9,11,13,15,17-octaenoic acidHCID 6437702—
Product9-((3Z)-Non-3-en-1-yl)-10-octylnonadecanedioic acidHCID 2283334220%

Reaction Conditions

Temperature200 °C

Reaction Steps

Employing the procedure of Example I, an amidoamine oxide was prepared from a polymeric fatty acid containing 87% C36 dimer acid and 13% trimer acid. For the reaction 352.2 gms of the polymeric fatty acid (Empol® 1016) was combined with 30 mls xylene, heated to 200° C. under a nitrogen atmosphere and 147.2 gms (20% equivalents excess) dimethylaminopropylamine added over a 2 hour period. Heating was continued at 200° C. while removing water until the acid value was 2.3. The reaction was terminated at that point and the xylene removed by vacuum distillation. One-hundred and seventy grams of the resulting amidoamine product was then dispersed in water (1000 mls) and reacted with 30% hydrogen peroxide (55.5 gms). The amber liquid product (14.5% solids) was slightly less viscous than the product obtained in Example I, possibly due to the lower solids content. Similar results are obtained when a polymeric fatty acid containing 80% C54 trimer acid and 20% C36 dimer acid is employed.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04367151
Source datasetuspto-grants-1983_01
ORD IDord-0ddce491e81c4d5fa62ada19cd3546b6
Source noteuspto-grants-1983_01