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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 34833Erstellt: 25. Oktober 2026

Bromo(phenyl)acetic acid → 2-Bromo-2-phenylethanol

https://huagongshe.com/reaction/34833

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBromo(phenyl)acetic acidHCID 97919—
EduktDiboronHCID 6328200—
EduktOxolane--water (1/1)HCID 21881883—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-Bromo-2-phenylethanolHCID 578332—

Reaktionsschritte

To a stirred solution of 25 g of α-bromphenylacetic acid in 100 ml of dry tetrahydrofuran was added 151 ml of 1.0M diborane in tetrahydrofuran dropwise at 5° C. under argon over 30 minutes. This mixture was stirred overnight at room temperature, then cooled to 0° C. and 130 ml of tetrahydrofuran:water (1:1) was added dropwise. The mixture was then saturated with potassium carbonate and the tetrahydrofuran removed. The aqueous remainder was extracted three times with ether. The extracts were combined and dried. The residue was triturated with hexane and the solid collected giving the desired compound as white needles, mp 38°-39° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04762942
Quelldatensatzuspto-grants-1988_08
ORD IDord-b0f3831dca3c442fb30e53f98498613d
Quellennotizuspto-grants-1988_08