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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1632873Generated: November 1, 2026

p-Toluenesulfonic acid monohydrate → p-Toluenesulfonic acid

https://huagongshe.com/reaction/1632873

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 20442582HCID 20442582—
SolventAcetoneHCID 180—
Productp-Toluenesulfonic acidHCID 6101164%

Reaction Steps

1-(2-Acetylthioethyl)-5-triphenylmethylaminomethyltetrazole, (e) (300 mg) in acetone (3 ml) was cooled to -20° and treated with p-toluenesulphonic acid monohydrate (128 mg) in acetone (2 ml). The reaction mixture was allowed to warm to room temperature and stirred for 7 hours. The resultant colourless solid was filtered off to give the p-toluenesulphonic acid salt (f) (190 mg), m.p. 184°-185°, νmax (KBr)1680, 1235, 1225, 1170, 1150, 1130, 1042, 1015, 838, 688, 572 cm-1, (D2O) 2.28 (3H,s), 2.35 (3H,s), 3.34 (2H, t, J Ca 6 Hz), 7.30 (2H, d, J 9 Hz), 7.65 (2H, d, J 9 Hz)ppm. Other signals were obscured by the HOD signal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04477662
Source datasetuspto-grants-1984_10
ORD IDord-096d7aed045a4dfa8b13684490d2a1ce
Source noteuspto-grants-1984_10