HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dichloroethane → Methyl N-Hept-6-enoyl-3-methyl-L-valinate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | 6-Heptenoic acid | HCID 70705 | — |
| Reactant | HOAt | HCID 181649 | — |
| Reactant | Methyl L-tert-leucinate | HCID 11309583 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | Methyl N-Hept-6-enoyl-3-methyl-L-valinate | HCID 59571176 | 80.7% |
Reaction Steps
A solution of L-t-leucine methyl ester (1.00 g, 6.89 mmol), 6-heptenoic acid (1.06 g, 8.26 mmol), EDC (1.58 g, 8.26 mmol) and HOAt (1.23 g, 8.26 mmol) in DMF (10 mL) was stirred at RT for 2 hours. The reaction mixture was diluted with aqueous saturated NaHCO3 (30 mL), and extracted with EtOAc (3×50 mL). The combined organic layers were washed with water (3×30 mL), brine (20 mL), dried over Na2SO4, filtered and concentrated. The residue was chromatographed on silica (5-50% EtOAc/hexane), to give the title compound (1.42 g). LRMS (ESI) m/z 256.3 [(M+H)+; calcd for C14H26NO3: 256.2].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08377874B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-0a373c9ecad14416ac060d77a282403f |
| Source note | uspto-grants-2013_02 |