HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Benzyloxyacetyl-gamma-butyrolactone → HCID 178519082, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Benzyloxyacetyl-gamma-butyrolactone | HCID 11402054 | — |
| Reactant | HCID 178418806 | HCID 178418806 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178519082 | HCID 178519082 | 65.5% |
Reaction Steps
In 2.0 ml of ethanol were dissolved 1.83 g of 2-benzyloxyacetyl-γ-butyrolactone and 0.50 g of 3-amino-pyrazole. To the solution, were added 60 μl of a boron trifluoride methanol complex, and the mixture was stirred for 16.5 hours at room temperature. The solvent was distilled off under reduced pressure, and the residue was subjected to column chromatography on silica gel (elution solvent: hexane:ethyl acetate=1:1→1:2) to obtain 1.18 g (yield: 65.5%) of the intended product as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06057330 |
| Source dataset | uspto-grants-2000_05 |
| ORD ID | ord-e947f8a6ef544518bad999011475c016 |
| Source note | uspto-grants-2000_05 |