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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1020784Erstellt: 25. Oktober 2026

Hydrochloric Acid → 1,3-Dihydro-1-hydroxy-2,1-benzoxaborol-5-ol

https://huagongshe.com/reaction/1020784

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktWaterHCID 962—
EduktSodium borohydrideHCID 4311764—
Edukt5-Hydroxy-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehydeHCID 57689987—
LösungsmittelMethanolHCID 887—
Produkt1,3-Dihydro-1-hydroxy-2,1-benzoxaborol-5-olHCID 57968699—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Into a 100-mL 3-necked round-bottom flask purged and maintained with an inert atmosphere of nitrogen was placed a solution of 5-hydroxy-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde (5.5 g, 22 mmol, 1.0 equiv) in methanol (25 mL). This was followed by the addition of NaBH4 (1.24 g, 32.6 mmol, 1.5 equiv) in several batches at 0° C. The resulting solution was stirred for 10 min at 0° C., then it was concentrated under vacuum to get rid of half methanol at low temperature. To the residual solution was added water (6 mL) and HCl (6M, 14.5 mL) dropwise at 0° C. The resulting solution was stirred overnight at room temperature. Then it was concentrated under vacuum at low temperature to remove MeOH. The solid was collected by filtration. This resulted in 2.0 g of benzo[c][1,2]oxaborole-1,5(3H)-diol as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08716478B2
Quelldatensatzuspto-grants-2014_05
ORD IDord-56a1b6da687c4867a7bb0d3aa7aa6186
Quellennotizuspto-grants-2014_05