HuagongsheHuagongshe Chemistry Print Report · For research reference only
Heptane → Methyl 6-bromohex-2-enoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Heptane | HCID 8900 | — |
| Reactant | Lithium Bromide | HCID 82050 | — |
| Reactant | HCID 85444077 | HCID 85444077 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 6-bromohex-2-enoate | HCID 53811689 | 83% |
Reaction Steps
In an atmosphere of nitrogen, 6-chloro-2-hexenoic acid methyl ester (4Cl); 188.8 g {GC purity; 83.6%, pure amount; 157.9 g (0.971 mol)}, lithium bromide (126.5 g, 1.457 mol) and heptane (16 ml) were added to a 500 ml capacity flask, followed by stirring for 6 hours under heptane reflux. After completion of the reaction, heptane was added as an extraction solvent and water was added thereto to separate the organic layer. The solvent was evaporated under a reduced pressure using an evaporator, and then the residue was distilled under a reduced pressure (70 to 80° C./0.1 ton) to obtain 6-bromo-2-hexenoic acid methyl ester (4Br); 203.4 g {GC purity; 82.3%, pure amount (4Br); 167.5 g (0.809 mol, yield 83%/(4Cl)}.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08217192B2 |
| Source dataset | uspto-grants-2012_07 |
| ORD ID | ord-fc2f0be483fc4e008a53d25faa8aa40b |
| Source note | uspto-grants-2012_07 |