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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1261860Generated: November 2, 2026

Ammonia → Pentanoic acid, 5-amino-4-oxo-, 4-methylbenzenesulfonate

https://huagongshe.com/reaction/1261860

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantHydrochloric AcidHCID 313—
ReactantAminolevulinic Acid HydrochlorideHCID 123608—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
SolventWaterHCID 962—
ProductPentanoic acid, 5-amino-4-oxo-, 4-methylbenzenesulfonateHCID 11623627—

Reaction Steps

A column was charged with 180 ml of a strongly acidic ion exchange resin (AMBERLITE IR120B Na, manufactured by Japan Organo). The ion exchange resin was used after converting it from sodium ion type to hydrogen ion type through a hydrochloric acid treatment. Next, 36.00 g (215 mmol) of 5-aminolevulinic acid hydrochloride was dissolved in 1800 ml of ion exchange water and passed through said column, and then 1000 ml of ion exchange water was passed through the same. Next, 1 N aqueous ammonia was slowly passed through the same to collect 555 ml of yellow eluate. The thus collected eluate was mixed with 81.72 g (430 mmol) of p-toluenesulfonic acid monohydrate and concentrated using an evaporator. To the concentrated liquid, 400 ml of acetone was added, followed by vigorously stirring with a stirrer and then the mixture was allowed to stand still at 4° C. for 16 hours. The thus precipitated solid was recovered by suction filtration and washed with 400 ml of acetone. The thus obtained solid was dried under reduced pressure for 12 hours to obtain 47.78 g (158 mmol) of the substance of interest. Its physical property data are shown below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08471061B2
Source datasetuspto-grants-2013_06
ORD IDord-0c3f8c1b5ffc4837bf06d94cafe2ac45
Source noteuspto-grants-2013_06