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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706195Generated: October 27, 2026

Acetic Acid → p-Toluenesulfonic acid

https://huagongshe.com/reaction/1706195

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantMethaneHCID 297—
ReactantHydrochloric AcidHCID 313—
Reactantdibutyl 3-[N-(p-methoxybenzyloxy)-N-tosylamino]propylphosphonateHCID 20185706—
SolventWaterHCID 962—
Productp-Toluenesulfonic acidHCID 6101—
Product3-(Hydroxyamino)propylphosphonic acidHCID 342170—

Reaction Steps

A mixture of dibutyl 3-[N-(p-methoxybenzyloxy)-N-tosylamino]propylphosphonate (28.4 g), 6 N hydrochloric acid (280 ml) and acetic acid (280 ml) was refluxed with stirring for 20 hours. The resultant mixture was concentrated under reduced pressure to give a residue, and then water was added thereto. The mixture was treated with an activated charcoal, whereafter the mixture was concentrated under reduced pressure to give an oily residue. The oily residue was washed with ether and dried under reduced pressure. The solid was washed with acetonitrile and ethyl ether to give p-toluenesulfonic acid salt of 3-(N-hydroxyamino)propylphosphonic acid (12.4 g) in the form of crystals. MP: 129°-135° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04206156
Source datasetuspto-grants-1980_06
ORD IDord-f7a42df1d7974c5ebc4161bbe7bc130d
Source noteuspto-grants-1980_06