HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenol → HCID 178431933, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | 3-Oxo-2-phenylprop-2-enoyl chloride | HCID 10773734 | — |
| Reactant | HCID 178431949 | HCID 178431949 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 178431933 | HCID 178431933 | — |
Reaction Steps
A stirred solution of 1.80 g. of phenyl chlorocarbonyl ketene (U.S. Pat. No. 3,679,801) in 20 ml. of chloroform is cooled to -40° C., and then 0.94 g of phenol is added. Stirring is con tinued at -40° C. for a further 20 minutes, and then a solution of 2.40 g. of 6-amino-2,2-dimethyl-3-(5-tetrazolyl)penam and 1.40 ml of triethylamine in 50 ml. of chloroform is added dropwise. The cooling bath is removed, and the mixture is stirred for a further 30 minutes. The mixture is filtered, and the chloroform is evaporated in vacuo to give crude 6-(2-phenoxycarbonyl-2-phenylacetamido)-2,2-dimethyl-3-(5-tetrazolyl)penam, as its triethylamine salt.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04179511 |
| Source dataset | uspto-grants-1979_12 |
| ORD ID | ord-4cb96a4743a74a1ba591f728e1b41a51 |
| Source note | uspto-grants-1979_12 |