HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → n-[1-Eth-(z)-ylidene-2,5-dioxo-pentyl]-acrylimidoyl bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | n-[1-Eth-(z)-ylidene-5,5-dimethoxy-2-oxo-pentyl]acrylimidoyl bromide | HCID 87233323 | — |
| Solvent | Water | HCID 962 | — |
| Product | n-[1-Eth-(z)-ylidene-2,5-dioxo-pentyl]-acrylimidoyl bromide | HCID 87233280 | 88.1% |
Reaction Steps
To a solution of N-[1-Eth-(Z)-ylidene-5,5-dimethoxy-2-oxo-pentyl]acrylimidoyl bromide (7.0 g, 28.9 mmol) in a solution of acetone (30 mL) and water (1.5 mL) at room temperature, is added Amberlyse-15 (20 g). After mechanical shacking for 3 hr at room temperature, the reaction mixture is filtered. The resin beads were washed with acetone (contain 10% of Et3N). The combined organic layers were concentrated and purified by chromatography (Hexane/EtOAc: 70/30) to yield N-[1-Eth-(Z)-ylidene-2,5-dioxo-pentyl]-acrylimidoyl bromide (5.18 g, 88.1%) as light yellow liquid. M/Z=421, 243.9 [M+1]
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08207183B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-06c6a7429ca748f58d34d22967db9e31 |
| Source note | uspto-grants-2012_06 |