HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1275404Generated: October 30, 2026
Triethylamine → (R)-2-Heptyl-pent-4-enoic acid dimethylamide
https://huagongshe.com/reaction/1275404
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Dimethylamine, hydrochloride | HCID 10473 | — |
| Reactant | Diethyl cyanophosphonate | HCID 76257 | — |
| Reactant | (2R)-2-Heptyl-pent-4-enoic acid | HCID 11041739 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (R)-2-Heptyl-pent-4-enoic acid dimethylamide | HCID 54259984 | 100.8% |
Reaction Steps
To a mixture of 5.00 g (0.025 mol) of the product of Example 5 and 2.27 g (0.028 mol) of dimethylamine hydrochloride in DMF at 0° C. was added 4.2 mL (0.028 mol) of diethyl cyanophosphonate followed by 7.38 mL (0.053 mol) of triethylamine. The reaction mixture was stirred at 0 degrees for 1 h and then at room temperature for 3 h. The resulting pale yellow suspension was diluted with 750 mL of EtOAc/Hex (2:1) and this solution was then washed with 5% aqueous HCl solution, water, saturated sodium bicarbonate and brine. The organic layer was dried over magnesium sulfate, filtered and concentrated in vacuo. The residue was chromatographed on silica gel eluting with ethyl acetate/hexanes (1:4) to provide 5.68 g (100%) of the title compound as a colorless oil. CI Mass Spec: 226.3 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06160132 |
|---|
| Source dataset | uspto-grants-2000_12 |
|---|
| ORD ID | ord-b3759146f281494786521db3a7c9c331 |
|---|
| Source note | uspto-grants-2000_12 |
|---|