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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1448370Generated: October 27, 2026

p-Toluenesulfonic acid monohydrate → p-Toluenesulfonic acid

https://huagongshe.com/reaction/1448370

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant6-(Triphenylmethylamino)-2,2-dimethyl-3-(1-furfuryltetrazol-5-yl)penamHCID 70605068—
SolventAcetoneHCID 180—
Productp-Toluenesulfonic acidHCID 6101—
Product6-Amino-2,2-dimethyl-3-(1-furfuryltetrazol-5-yl)penamHCID 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 (β-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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04179511
Source datasetuspto-grants-1979_12
ORD IDord-296ad37645dc4445af979b36019b5675
Source noteuspto-grants-1979_12