HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hexylamine → L-pyroglutamic acid n-hexyl amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hexylamine | HCID 8102 | — |
| Reactant | 2,4,5-Trichlorophenyl 5-oxo-L-prolinate | HCID 111108 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | L-pyroglutamic acid n-hexyl amide | HCID 54158437 | — |
Reaction Steps
4 ml of n-hexyl amine were added at 0° C. to a solution of 3.1 g of L-pyroglutamic acid 2,4,5-trichlorophenyl ester in 10 ml of dimethyl formamide and the solution was left at room temperature for 20 hours. The solvent was removed by distillation in vacuo at room temperature. The residue was taken up in 90% aqueous methanol, and the solution was filtered successively through 200 ml each of Levatit S 100(H+ -form)and Serdolit Blau (OH- -form). The ion exchanger columns were washed with 200 ml of 90% methanol and the combined eluate and washing solution were concentrated in vacuo. The L-pyroglutamic acid n-hexyl amide obtained as a colorless solid was recrystallized from ethyl acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04053588 |
| Source dataset | uspto-grants-1977_10 |
| ORD ID | ord-9605a953e7554adc979b013a2dfb99e5 |
| Source note | uspto-grants-1977_10 |