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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750855Generated: October 31, 2026

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

https://huagongshe.com/reaction/1750855

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 numberUS09156860B2
Source datasetuspto-grants-2015_10
ORD IDord-2fe8958d648249e789fa73ffbb86a22e
Source noteuspto-grants-2015_10