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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 333209Erstellt: 23. Oktober 2026

Chloroform → HCID 73297273, Verbindung

https://huagongshe.com/de/reaction/333209

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChloroformHCID 6212—
EduktPotassium CarbonateHCID 11430—
EduktBromoacetyl bromideHCID 61147—
Edukt2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)anilineHCID 2734652—
LösungsmittelWaterHCID 962—
LösungsmittelHexaneHCID 8058—
LösungsmittelEthyl AcetateHCID 8857—
ProduktHCID 73297273HCID 73297273—

Reaktionsschritte

(50 g, 0.228 mol) of 2-aminophenyl boronic acid pinacol ester and (110 g, 0.798 mole) of potassium carbonate were charged into 10 L, 3 necks RBF connected with overhead stirrer, thermometer and additional funnel, 5 L of Chloroform, synthetic grade was loaded then stirred for 10±5 minutes at 25±5° C. after that (115 g, 50 mL, 0.57 mol) of Bromoacetyl bromide was added drop wise during 10±5 minutes while the mixture stirred. After end of loading, the mixture was stirred for 1-2 hrs at 25±5° C., the reaction completion was monitored by TLC (Ethyl acetate:n-hexane, 15:85 v/v). Afterward, 4-5 L of purified water was loaded then transferred to 10 L separatory funnel and steeled down for 10 minutes, chloroform layer (lower) was separated and dried over 50 g of sodium sulfate and filtered. The filtrate solution was concentrated under vacuum to dryness. The residue was recrystallized from diethyl ether to get pure 2-(bromoacetamido)phenylboronic acid intermediate, the product was characterized by 1H-NMR, 13C-NMR, mass and elemental analysis.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08877980B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-bcbbc28f85c3442f9c5b2c2a25c38c4c
Quellennotizuspto-grants-2014_11