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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1658028Generated: October 31, 2026

Cyclohexane → p-Methoxybenzyl alpha-amino-dimethylphosphonoacetate

https://huagongshe.com/reaction/1658028

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexaneHCID 8078—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactantp-methoxybenzyl N-benzylidene-alpha-amino-dimethylphosphonoacetateHCID 54064440—
SolventDiethyl EtherHCID 3283—
Productp-Methoxybenzyl alpha-amino-dimethylphosphonoacetateHCID 21529965—

Reaction Steps

p-Methoxybenzyl N-benzylidene-α-amino-dimethylphosphonoacetate (9.78 g) in ether (50 ml) is added over 20 minutes to a stirring solution of p-toluenesulfonic acid monohydrate (4.76 g) in ether (150 ml). Cyclohexane (100 ml) is added and the solvents are decanted off. The residue is washed with more 2:1 ether-cyclohexane, which is again decanted off. The residue is partitioned between methylene chloride and 1 M dipotassium hydrogen phosphate (50 ml). The organic portion is separated, washed with water, dried, and evaporated in vacuo to give p-methoxybenzyl α-aminodimethylphosphonoacetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03962224
Source datasetuspto-grants-1976_06
ORD IDord-68f825aa3f964ab7a444afb4f4d7046b
Source noteuspto-grants-1976_06