HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitrogen → Benzyl 4-ethoxycarbonylmethoxybutyrate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Ethyl diazoacetate | HCID 12192 | — |
| Reactant | Benzyl 4-hydroxybutanoate | HCID 14443958 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | Benzyl 4-ethoxycarbonylmethoxybutyrate | HCID 18991532 | — |
Reaction Steps
65 g (0.33 mol) of benzyl 4-hydroxybutyrate and 260 mg of copper powder are charged to 120 ml of cyclohexane and the mixture is heated to reflux. Then a mixture of 38.7 ml (0.37 mol) of ethyl diazoacetate and 300 ml of cyclohexane are added, whereupon evolution of N2 ensues. The reaction mixture is stirred for 4 hours under reflux and then for 4 hours at room temperature, filtered over a glass fibre filter and concentrated by evaporation. The residue is chromatographed on silica gel with hexane/ethyl acetate 4:1, giving benzyl 4-ethoxycarbonylmethoxybutyrate as a colourless liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05294734 |
| Source dataset | uspto-grants-1994_03 |
| ORD ID | ord-c64a5e4c4e5c468fbf78a15e26caa6f7 |
| Source note | uspto-grants-1994_03 |