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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284469Generated: October 26, 2026

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

https://huagongshe.com/reaction/2284469

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
Reactant5-Hydroxy-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehydeHCID 57689987—
SolventMethanolHCID 887—
Product1,3-Dihydro-1-hydroxy-2,1-benzoxaborol-5-olHCID 57968699—

Reaction Conditions

Temperature0 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145429B2
Source datasetuspto-grants-2015_09
ORD IDord-17938e693da34a6c993d369cd2a14a95
Source noteuspto-grants-2015_09