HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Chloride → N-Farnesyl farnesyl carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | Farnesylamine | HCID 3080630 | — |
| Reactant | 4,8,12-Trimethyltrideca-3,7,11-trienoic acid | HCID 53791761 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | N-Farnesyl farnesyl carboxamide | HCID 54142715 | 86.4% |
Reaction Steps
To a mixture of farnesyl carboxylic acid (7.15 g) and farnesylamine (6.95 g) in 20 ml of dimethylformamide was added at 0° C. to a solution of diphenylphosphorylazide (7.62 g) in 7 ml of dimethylformamide. Next, to this mixture was added a solution of triethylamine (3.20 g) in dimethylformamide (3 ml). The reaction mixture was kept at room temperature overnight and poured into water (900 ml). After adding table salt, this mixture was extracted with ethyl acetate. The organic phase was worked up as usual manner and gave pale yellow oil. This material was purified by silica gel chromatography by using a mixture of methanol:benzene (2:1) as the eluent and gave 11.20 g of the titled compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04520029 |
| Source dataset | uspto-grants-1985_05 |
| ORD ID | ord-f5af81d0a344424c9e5b04c3e70b00f5 |
| Source note | uspto-grants-1985_05 |