HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromodecane → N-(2-methoxy-2-oxoethyl)-N-[3,5-bis(decyloxy) phenyl]glycine methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromodecane | HCID 8173 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 19389065 | HCID 19389065 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | N-(2-methoxy-2-oxoethyl)-N-[3,5-bis(decyloxy) phenyl]glycine methyl ester | HCID 15232831 | 52.8% |
Reaction Steps
A mixture of 0.50 g (1.86 mmol) of N-[(3,5-Dihydroxy)phenyl]-N-(2-methoxy-2-oxoethyl)glycine methyl ester, 0.81 ml (3.9 mmol) of 1-bromodecane and 0.77 g (5.57 mmol) of potassium carbonate in 15 ml of acetone was stirred at reflux for 24 hours. An additional 0.8 ml of 1-bromodecane was added and reflux was continued for 48 hours. The reaction mixture was filtered through a Celite pad and the filtrate was concentrated at reduced pressure to an oil which was purified by HPLC using 15% ethyl acetate-hexane to give 0.54 g (52% yield) of N-(2-methoxy-2-oxoethyl)-N-[3,5-bis-(decyloxy)phenyl]glycine methyl ester as an oil. The nmr and mass spectra of this product were identical to those obtained using the procedure of Example 5.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05324747 |
| Source dataset | uspto-grants-1994_06 |
| ORD ID | ord-73af0fc200664312b4b71f9c137f43f3 |
| Source note | uspto-grants-1994_06 |