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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 451633Generated: October 29, 2026

Sulfuric Acid → HCID 86656427, compound

https://huagongshe.com/reaction/451633

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
Reactant4-(4-Aminophenyl)butanoic acidHCID 27049—
ReactantHCID 14451767HCID 14451767—
SolventMethanolHCID 887—
ProductHCID 86656427HCID 8665642784%

Reaction Conditions

Temperature50 °C

Reaction Steps

The 4-aminophenylbutyramide used in this example was obtained according to patent literature WO 02/08247 A2 or WO 03/051909 A2. Procedure was as follow: Methanol (100 ml) was charged to 4-(4-Aminophenyl)-butyric acid (from Aldrich) CAS[15118-60-2] (FW=179.22, 1 eq, 15 g, 83.7 mmol). Sulphuric acid FW=98.08 (4 eq, 334.8 mmol, 33 g) was added maintaining the temperature below 20° C. The mixture was then refluxed for one hour and concentrated by distillation at atmospheric pressure until half of methanol will be removed. The reaction mixture was then cooled to 50° C. and t-butyl-methyl ether was added maintaining the temperature above 45° C. The mixture was then gradually cooled to 0-5° C. and held at this temperature for 1 hour. The resultant crystalline product was isolated by filtration and washed by cold mixture of methanol and t-butyl-methyl ether (4:10) and cold ether and then dried under vacuum and then dried under vacuum to give methyl 4-aminophenylbutyrate hydrogensulfate as a white crystal (20.0 g, 84%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08487130B2
Source datasetuspto-grants-2013_07
ORD IDord-87ab5f99bed74880ad8cc41afd30cf7b
Source noteuspto-grants-2013_07