HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → Butyl α-[[(1,1-dimethylethoxy)carbonyl]amino]-2-furanacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Furan | HCID 8029 | — |
| Reactant | HCID 20312395 | HCID 20312395 | — |
| Catalyst | Boron trifluoride etherate | HCID 8000 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Butyl α-[[(1,1-dimethylethoxy)carbonyl]amino]-2-furanacetate | HCID 54559425 | — |
Reaction Steps
A solution of 1.6 g. (0.006 mol.) of N-t-butoxycarbonyl-2-acetoxyglycine n-butyl ester and 0.7 g. (0.01 mol.) of redistilled furan in 75 ml. of methylene chloride was cooled to -78° and four drops of boron trifluoride etherate was added with stirring. The reaction mixture was warmed to room temperature and left for three hours. Chromatography on silica gel with methylene chloride and methylene chloride containing increasing amounts of ethyl acetate gave the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03997584 |
| Source dataset | uspto-grants-1976_12 |
| ORD ID | ord-c199a5d5d2354edb9410bbaa6249cafd |
| Source note | uspto-grants-1976_12 |