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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 532143Generated: November 1, 2026

Hydrochloric Acid → 1-Hydroxy-3,3-dimethyl-1,3-dihydrobenzo[c][1,2]oxaborole-5-carbaldehyde

https://huagongshe.com/reaction/532143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzoyl PeroxideHCID 7187—
ReactantSodium CarbonateHCID 10340—
ReactantN-bromobutanimideHCID 67184—
Reactant3,3,5-Trimethylbenzo[c][1,2]oxaborol-1(3h)-olHCID 76847953—
SolventCarbon TetrachlorideHCID 5943—
Product1-Hydroxy-3,3-dimethyl-1,3-dihydrobenzo[c][1,2]oxaborole-5-carbaldehydeHCID 76847491412.8%

Reaction Steps

To a solution of 3,3,5-trimethylbenzo[c][1,2]oxaborol-1(3H)-ol (27 mg, 0.153 mmol) in CCl4 (2 mL) at rt was added benzoyl peroxide (3.7 mg, 0.0153 mmol) followed by NBS (60 mg, 0.337 mmol). The reaction mixture was heated under reflux for 12 h, cooled to rt and treated with Na2CO3. The aqueous layer was acidified with 3 N HCl to pH of 3 and extracted with EA. The organic layer was washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by prep-TLC to give 1-hydroxy-3,3-dimethyl-1,3-dihydrobenzo[c][1,2]oxaborole-5-carbaldehyde (12 mg; yield 41%) as white solid. 1H NMR (400 MHz, CDCl3): δ 10.12 (s, 1 H), 7.88 (s, 2 H), 7.80 (s, 1 H), 1.62 (s, 6 H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853186B2
Source datasetuspto-grants-2014_10
ORD IDord-62ed1e4700ce47419af5e29c8bb6b792
Source noteuspto-grants-2014_10