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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1283692Generated: October 31, 2026

p-Toluenesulfonic acid → HCID 131710049, compound

https://huagongshe.com/reaction/1283692

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantHCID 131710048HCID 131710048—
SolventAcetoneHCID 180—
ProductHCID 131710049HCID 13171004964.7%

Reaction Steps

t-Butyl 3-p-fluorobenzyl-7-triphenylmethylamino-3-cephem-4-carboxylate (IX) (72 mg) was dissolved in acetone and the solution cooled to 0°. p-Toluene sulphonic acid (25 mg) in acetone (0.5 ml) was added dropwise over a few minutes and the solution left to warm to room temperature with stirring. After 2.5 hours a solid had formed but t.l.c. still showed some unchanged (IX) to be present. The mixture was again cooled to 0° and a further quantity of p-toluene sulphonic acid (5 mg) in acetone added. After leaving at room temperature for a further 1.5 hours, the white solid was filtered off. This solid was suspended in ethyl acetate and treated with saturated sodium bicarbonate solution. The organic layer was washed with brine, dried and evaporated to give t-butyl 7-amino-3-p-fluorobenzyl-3-cephem-4-carboxylate (XI) (28 mg) shown to be pure by t.l.c. ##SPC17##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03975383
Source datasetuspto-grants-1976_08
ORD IDord-db2f173d6d3d4558ad6282e87ff7ee9c
Source noteuspto-grants-1976_08