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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 532218Generated: October 31, 2026

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

https://huagongshe.com/reaction/532218

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzoyl PeroxideHCID 7187—
ReactantSodium CarbonateHCID 10340—
ReactantN-bromobutanimideHCID 67184—
Reactant3,3-diethyl-5-methylbenzo[c][1,2]oxaborol-1(3H)-olHCID 86685083—
SolventCarbon TetrachlorideHCID 5943—
Product3,3-Diethyl-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborole-5-carbaldehydeHCID 86685084561.5%

Reaction Steps

To a solution of 3,3-diethyl-5-methylbenzo[c][1,2]oxaborol-1(3H)-ol (2.0 g, 9.8 mmol) in CCl4 (25 ml) at rt was added benzoyl peroxide (237 mg, 0.98 mmol) followed by NBS (3.489 g, 19.6 mmol). The reaction mixture was refluxed for 16 h, cooled to rt and treated with aqueous Na2CO3. The aqueous layer was acidified with 3N HCl to pH=3 and extracted with EA (50 ml×3). The organic layer was washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure to give the desired product (1.2 g, yield 56%) as white solid. 1H NMR (300 MHz, DMSO-d6): δ 10.06 (s, 1H), 9.30 (s, 1H), 7.85 (m, 3H), 1.86 (m, 4H), 0.55 (m, 6H). MS: m/z=219 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853186B2
Source datasetuspto-grants-2014_10
ORD IDord-47be4f210347480484acee3b8895408e
Source noteuspto-grants-2014_10