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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721548Generated: November 3, 2026

Hydrochloric Acid → HCID 131719389, compound

https://huagongshe.com/reaction/1721548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcryloyl chlorideHCID 13140—
Reactant2-Hydroxyethyl MethacrylateHCID 13360—
ReactantAcrylateHCID 25188—
Reactant2-Amino-6-(((tert-butoxy)carbonyl)amino)hexanoic acidHCID 544580—
Reactant4-Benzoylbenzoyl chlorideHCID 12912141—
CatalystAzobisisobutyronitrileHCID 6547—
SolventEthanolHCID 702—
SolventBicarbonate IonHCID 769—
SolventEthyl AcetateHCID 8857—
ProductHCID 131719389HCID 131719389—

Reaction Steps

4-Benzoylbenzoyl-lysyl-acrylate (BBA-LYS-AC) is prepared by reacting N-epsilon-t-BOC-L-lysine with 4-benzoylbenzoyl chloride, then deblocking the epsilon-amino group with 3N HCl in ethyl acetate for one hour at room temperature followed by reaction with acryloyl chloride at pH 9.0. This reagent is coated onto silicone contact lenses by incubating the reagent solution in 50% ethanol in 0.1M bicarbonate buffer at pH 9.5 for two hours at room temperature, then exposing to high intensity light at 305 nm. The acrylate is the polymerization site. A solution of 5% hydroxyethylmethacrylate in 0.1M bicarbonate buffer at pH 9.0 is then polymerized on the lenses using 2,2'-azobisisobutyronitrile as catalyst. The polymerization reaction is allowed to proceed for one hour at room temperature, after which the uncoupled polymer is removed by washing the plates. This procedure improves wettability of the lenses.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05512329
Source datasetuspto-grants-1996_04
ORD IDord-1190880cae1a4817a969c90c3452a429
Source noteuspto-grants-1996_04