Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1950704Generated: October 30, 2026

Sulfuric Acid → L-Hydroxyproline

https://huagongshe.com/reaction/1950704

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantPotassium ChlorideHCID 4873—
Reactant4-(Dimethylamino)BenzaldehydeHCID 7479—
ReactantBoric AcidHCID 7628—
ReactantPotassium HydroxideHCID 14797—
ReactantTosylchloramideHCID 31388—
ReactantL-Proline, 1-hydroxyHCID 22795248—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Solvent2-MethoxyethanolHCID 8019—
ProductL-HydroxyprolineHCID 5810—
Product4-(Dimethylamino)BenzaldehydeHCID 7479—
ProductBoric AcidHCID 7628—
ProductTosylchloramideHCID 31388—

Reaction Steps

A boric acid buffer was prepared by dissolving 6.18 g of boric acid and 22.5 g of KCl in distilled water, adjusting at pH 8.7 with potassium hydroxide and making the total volume 100 ml. A chloramine T solution was prepared by dissolving 1.41 g of chloramine T (NACALAITESQUE, Catalog No.080-05) in 25 ml of 2-methoxyethanol (NACALAITESQUE, Catalog No.153-10). A p-dimethylaminobenzaldehyde solution was prepared by dissolving 12 g of p-dimethylaminobenzaldehyde (NACALAITESQUE, Catalog No.128-16) in 20 ml of ethanol followed by adding a mixture of 2.74 ml of concentrated sulfuric acid and 20 ml of ethanol slowly to the solution with cooling on ice. A hydroxyproline conventional solution was prepared by dissolving 3 mg of hydroxy-L-proline (NACALAITESQUE, Catalog No.188-17) in 1 ml of distilled water (3 mg/ml).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404652B2
Source datasetuspto-grants-2013_03
ORD IDord-71abd08380f64e7f8f88462895fd8297
Source noteuspto-grants-2013_03