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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2419351Generated: October 27, 2026

p-Toluenesulfonic acid monohydrate → p-Toluenesulfonic acid

https://huagongshe.com/reaction/2419351

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 (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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04105668
Source datasetuspto-grants-1978_08
ORD IDord-6580a5c560314fad8637ea2affd15a56
Source noteuspto-grants-1978_08