HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1580486Generated: November 1, 2026
p-Toluenesulfonic acid → HCID 131709915, compound
https://huagongshe.com/reaction/1580486
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Anisole | HCID 7519 | — |
| Reactant | HCID 70524001 | HCID 70524001 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 131709915 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03932465 |
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| Source dataset | uspto-grants-1976_01 |
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| ORD ID | ord-843501dac3aa4d3ca68e96fa74581f6c |
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| Source note | uspto-grants-1976_01 |
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