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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 532235Generated: October 30, 2026

Hydrochloric Acid → 6-Fluoro-1-hydroxy-3,3-dimethyl-1,3-dihydrobenzo[c][1,2]oxaborole-5-carbaldehyde

https://huagongshe.com/reaction/532235

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzoyl PeroxideHCID 7187—
ReactantSodium CarbonateHCID 10340—
ReactantN-bromobutanimideHCID 67184—
Reactant6-fluoro-3,3,5-trimethylbenzo[c][1,2]oxaborol-1(3H)-olHCID 86685095—
SolventCarbon TetrachlorideHCID 5943—
Product6-Fluoro-1-hydroxy-3,3-dimethyl-1,3-dihydrobenzo[c][1,2]oxaborole-5-carbaldehydeHCID 86685097908.7%

Reaction Steps

To a solution of 6-fluoro-3,3,5-trimethylbenzo[c][1,2]oxaborol-1(3H)-ol (388 mg, 2 mmol) in CCl4 (60 mL) at rt was added benzoyl peroxide (48.4 mg, 0.2 mmol) followed by NBS (783 mg, 4.4 mmol). The reaction mixture was heated under reflux for 16 h, cooled to rt and treated with Na2CO3. The aqueous layer was acidified with 3 N HCl to pH of 3 and extracted with DCM (60 mL×3). The organic layer was dried over Na2SO4, filtered and concentrated under reduced pressure to give 6-fluoro-1-hydroxy-3,3-dimethyl-1,3-dihydrobenzo[c][1,2]oxaborole-5-carbaldehyde (378 mg, 91%) as a pale yellow solid. 1H NMR (500 MHz, CDCl3) δ 10.369 (s, 1H), 7.687 (d, J=5.5 Hz, 1H), 7.409 (d, J=8.0 Hz, 1H), 2.715 (s, 3H), 1.484 (s, 6H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853186B2
Source datasetuspto-grants-2014_10
ORD IDord-57f84abaf0f04eaa99c5ab6f1914b610
Source noteuspto-grants-2014_10