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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1448371Generated: November 2, 2026

p-Toluenesulfonic acid monohydrate → HCID 70604552, compound

https://huagongshe.com/reaction/1448371

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 70604632HCID 70604632—
SolventAcetoneHCID 180—
ProductHCID 70604552HCID 7060455254%

Reaction Steps

To a stirred solution of 1.827 g. of 6-(triphenylmethylamino)-2,2-dimethyl-3-(1-[5-methylfurfuryl]tetrazol-5-yl)penam in 3 ml. of acetone is added a solution of 0.59 g. of p-toluenesulfonic acid monohydrate in 2 ml. of acetone. The mixture is stirred at ambient temperature for 30 minutes, and then the precipitate which has formed is filtered off. This affords 0.87 g. (54% yield) of the title compound as its p-toluenesulfonate salt. The NMR spectrum of the product (CDCl3) shows absorptions at 7.28 ppm (q, 4H), 6.50 ppm (d, 1H), 6.01 ppm (s, 1H), 5.86 ppm (s, 2H), 5.71 ppm (s, 1H), 5.68 ppm (d, 1H), 5.09 ppm (d, 1H), 2.00 ppm (2s, 6H), 1.66 ppm (s, 3H) and 0.88 ppm (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04179511
Source datasetuspto-grants-1979_12
ORD IDord-955c4543730f4036859f57156bdafbd7
Source noteuspto-grants-1979_12