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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1580486Generated: November 1, 2026

p-Toluenesulfonic acid → HCID 131709915, compound

https://huagongshe.com/reaction/1580486

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantAnisoleHCID 7519—
ReactantHCID 70524001HCID 70524001—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 131709915HCID 131709915—

Reaction Steps

A solution of 0.044 g of anisole and 0.0172 g of p-toluenesulphonic acid in 2 ml of anhydrous dioxane is mixed with 0.035 g of 3-hydroxymethyl-7-(N-phenylacetyl-amino)-ceph-2-em-4ξ-carboxylic acid and the resulting solution is left to stand for one hour at room temperature. The solvent is removed under reduced pressure and the residue is triturated with diethyl ether to remove the excess of p-toluenesulphonic acid and is worked up in accordance with the process described in example 6. 3-(4-Methoxy-benzyl)-7-(N-phenylacetyl-amino)-ceph-2-em-4ξ-carboxylic acid containing a small amount of the corresponding 2-methoxybenzyl compound is thus obtained; in a thin layer chromatogram, this acid does not differ from the product of the process of example 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03932465
Source datasetuspto-grants-1976_01
ORD IDord-843501dac3aa4d3ca68e96fa74581f6c
Source noteuspto-grants-1976_01