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 3 hours. Chromotography 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 | US04108854 |
| Source dataset | uspto-grants-1978_08 |
| ORD ID | ord-573683eb7cb1427fbb9b8272e3d65d03 |
| Source note | uspto-grants-1978_08 |