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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1658022Generated: October 31, 2026

Cyclohexane → HCID 54227761, compound

https://huagongshe.com/reaction/1658022

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexaneHCID 8078—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 54211819HCID 54211819—
SolventDiethyl EtherHCID 3283—
ProductHCID 54227761HCID 54227761—

Reaction Steps

A solution of p-nitrobenzyl N-benzylidene-α-aminodiphenylphosphonoacetate (16.43 g) in ethyl ether (100 ml) is added dropwise over 30 minutes to a stirring solution of p-toluenesulfonic acid monohydrate (6.48 g) in ethyl ether (150 ml). Cyclohexane (100 ml) is added to the mixture and the solvents are decanted from the precipitate. The precipitate is washed with more 2:1 ethyl ether-cyclohexane which is again decanted off. The precipitate is treated with 1 M aqueous dipotassium hydrogen phosphate (60 ml) and extracted with four portions of methylene chloride. The methylene chloride solution is dried over magnesium sulfate, filtered, and evaporated to give p-nitrobenzyl α-aminodiphenylphosphonacetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03962224
Source datasetuspto-grants-1976_06
ORD IDord-6722a63cf2ac4628b79726730a1a5ee2
Source noteuspto-grants-1976_06