Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Phenyl chloroformate | HCID 15891 | — |
| Reactant | Sodium Bromide | HCID 253881 | — |
| Reactant | Methanol--water (1/1) | HCID 22242641 | — |
| Product | HCID 22765908 | HCID 22765908 | — |
Reaction Steps
Phenyl N,N-dimethylformamide bromide was prepared by dropwise addition of phenyl chloroformate (6.5 ml; 50 mmol) to a stirred solution of sodium bromide (5.14 g; 50 mmol) in dimethylformamide at 0°-5° C. Sodium chloride precipitated, and the resulting suspension was stirred at 0°-5° C. for 4 hours and then at room temperature overnight. The mixture was cooled to 0° C. and 16-deacetoxy-16β-(acetylthio)fusidic acid acetoxymethyl ester (6.07 g; 10 mmol) was added with stirring. After stirring at 0°-5° C. for 4 hours, the mixture was left at room temperature for a further 4 days. On dilution of the stirred reaction mixture with methanol-water 1:1 (75 ml) an oily product precipitated, which was washed repeatedly by decantation with methanol-water 1:1 and finally taken up in ether, dried, and evaporated in vacuo. The amorphous residue thus obtained was purified by dry column chromatography on silica gel (petroleum ether-ethyl acetate 85:15) to give the desired compound as a colourless foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04119717 |
|---|
| Source dataset | uspto-grants-1978_10 |
|---|
| ORD ID | ord-97e0a625f9c64beba09efdec33590f85 |
|---|
| Source note | uspto-grants-1978_10 |
|---|