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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 232750Erstellt: 25. Oktober 2026

Trimethyl borate → Boronic acid, (4-ethylphenyl)-

https://huagongshe.com/reaction/232750

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrimethyl borateHCID 8470—
Edukt1-Bromo-4-ethylbenzeneHCID 15313—
EduktMagnesiumHCID 5462224—
LösungsmittelDiethyl EtherHCID 3283—
ProduktBoronic acid, (4-ethylphenyl)-HCID 273435241%

Reaktionsschritte

A solution of 1-bromo-4-ethyl benzene (2.0 g, 11 mmol) in dry ether (5 ml) was added to magnesium turnings (311 mg, 13 mmol), which had been suspended in dry ether, by a dropwise addition. After addition was complete, the suspension was refluxed for a period of 15 min after which nearly all of the magnesium had reacted. This solution was then added to trimethy borate (1.12 g, 11 mmol) previously dissolved in ether (5 ml) at -78° C., the solution was warmed to room temperature and stirred for 90 min. The reaction was quenched by the addition of 10% aqueous HCl (2 ml) and the solution was extracted with ether. The combined ether extracts was extracted with 1M NaOH (2×20 ml), the aqueous extracts were acidified with dilute HCl to pH 2 and extracted with ether (2×25 ml). The combined ether extracts was washed once with water (10 ml), dried and evaporated to produce a white solid (676 mg, 38% yield), m.p. 138°-140° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05591761
Quelldatensatzuspto-grants-1997_01
ORD IDord-c1c147a2cbeb4858ba5715228f5b065a
Quellennotizuspto-grants-1997_01