HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid monohydrate → p-Toluenesulfonic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | 6-(Triphenylmethylamino)-2,2-dimethyl-3-(1-furfuryltetrazol-5-yl)penam | HCID 70605068 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | p-Toluenesulfonic acid | HCID 6101 | — |
| Product | 6-Amino-2,2-dimethyl-3-(1-furfuryltetrazol-5-yl)penam | HCID 70604821 | — |
Reaction Steps
To a stirred solution of 0.422 g. (0.75 mmole) of 6-(triphenylmethylamino)-2,2-dimethyl-3(1-furfuryltetrazol-5-yl)penam in 1 ml of acetone at ambient temperature, is added 0.142 g. (0.75 mmole) of p-toluenesulfonic acid monohydrate. Stirring is continued for 30 minutes, and then the solvent is removed by evaporation in vacuo. This affords the title compound as its p-toluenesulfonate salt. IR (Nujol mull): 1780 cm-1 (B-lactam). NMR (DMSO-d6): 7.20 ppm (q,4H), 6.40 ppm (m,2H), 5.90 ppm (s,2H), 5.60 ppm (m,2H), 5.00 ppm (d,1H), 2.20 ppm (s,3H), 1.60 ppm (s,3H), 0.80 ppm (s,3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04105668 |
| Source dataset | uspto-grants-1978_08 |
| ORD ID | ord-6580a5c560314fad8637ea2affd15a56 |
| Source note | uspto-grants-1978_08 |