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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1501523Generated: November 3, 2026

Water → 2-Hydroxy-4,5-dimethoxybenzaldehyde

https://huagongshe.com/reaction/1501523

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3,4,5-TrimethoxybenzaldehydeHCID 6858—
ReactantBoron tribromideHCID 25134—
SolventDichloromethaneHCID 6344—
Product2-Hydroxy-4,5-dimethoxybenzaldehydeHCID 1098690887%

Reaction Conditions

Temperature0 °C

Reaction Steps

To solution of 3,4,5-trimethoxybenzaldehyde (5 g, 25.5 mmol) in CH2Cl2 (125 ml) at 0° C. was added BBr3 (6.39 g, 25.5 mmol). The resulting dark mixture was stirred at 0° C. for 10 hrs after completion of the reaction checked by TLC H2O (100 mL) was then added and the mixture was stirred for 10 min and the aqueous phase was extracted by CH2Cl2. The organic phase was dried over Na2SO4, and evaporated under reduced pressure. The resulting residue was purified by silica gel (CH2Cl2) afforded the 2-hydroxy 4,5dimethoxybenzaldehyde A1 (4.3 g) in 87% yield isolated yellow solid: 1H NMR (500 MHz, CDCl3) δ 11.33 (s, 1H), 9.63 (s, 1H), 6.83 (s, 1H), 6.40 (s, 1H), 3.87 (s, 3H), 3.81 (s, 3H) ppm. Mass: ESI [M+Na]+: 225.06; Elemental anal. calcd. for C9H10O4; C, 59.34; H, 5.53; O, 35.13. found C, 59.14; H, 5.13; O, 34.90.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206201B2
Source datasetuspto-grants-2015_12
ORD IDord-3a4db0d4238942bebacc8b4c16cdbd0c
Source noteuspto-grants-2015_12