HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl bromoacetate → Oleyl bromoacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl bromoacetate | HCID 60984 | — |
| Reactant | Oleyl Alcohol | HCID 5284499 | — |
| Product | Oleyl bromoacetate | HCID 56640678 | — |
Reaction Steps
Technical grade oleyl alcohol (85 wt %; 10 g; 37.2 mmol) was combined with Novozym 435 (200 mg) in an amber bottle. Methyl bromoacetate (6.84 g; 44.7 mmol; 1.2 equiv.) was added, and the mixture was sealed and stirred at room temperature overnight to afford about 50% conversion to oleyl bromoacetate. The mixture was then purged with a subsurface stream of nitrogen 2.5 days to afford 98.5% conversion of oleyl alcohol to oleyl bromoacetate according to GC analysis. The mixture was filtered, and the solid was washed with toluene. The filtrate was concentrated to give the desired product as a viscous colorless oil (13.19 g, 91%). The product was used in the subsequent reactions without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08846723B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-7b981f4a1b054da2a604a68cfd4aad30 |
| Source note | uspto-grants-2014_09 |