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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1658001Generated: November 4, 2026

p-Toluenesulfonic acid monohydrate → p-Toluenesulfonic acid

https://huagongshe.com/reaction/1658001

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactanttrichloroethyl N-benzylidene-alpha-amino-diethylphosphonoacetateHCID 54407468—
SolventDiethyl EtherHCID 3283—
Productp-Toluenesulfonic acidHCID 6101265.3%
ProductTrichloroethyl alpha-amino-diethylphosphonoacetateHCID 21529974—

Reaction Steps

A solution of trichloroethyl N-benzylidene-α-amino-diethylphosphonoacetate (5.69 g., 13.2 mmole) in ethyl ether (25 ml.) is added to a rapidly stirring solution of p-toluenesulfonic acid monohydrate (2.76 g., 14.5 mmole) in ethyl ether (75 ml.). A white precipitate appears immediately. The mixture is stirred for 10 minutes at room temperature, then cooled in ice. The product is collected by suction filtration, washed with cold ethyl ether, and dried in vacuo to give trichloroethyl α-aminodiethylphosphonoacetate, p-toluenesulfonate (6.03 g.) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03962224
Source datasetuspto-grants-1976_06
ORD IDord-8b5669a074844bd78201e8d398e0b43b
Source noteuspto-grants-1976_06