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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1632025Generated: October 31, 2026

Methane, dichloromethoxy- → 3-Bromo-2-fluoro-4-methoxybenzaldehyde

https://huagongshe.com/reaction/1632025

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethane, dichloromethoxy-HCID 21004—
Reactant2-Bromo-3-fluoroanisoleHCID 2779318—
CatalystTitanium TetrachlorideHCID 24193—
SolventDichloromethaneHCID 6344—
Product3-Bromo-2-fluoro-4-methoxybenzaldehydeHCID 5770373774%

Reaction Steps

In a 3-necked 250 mL round-bottomed flask equipped with nitrogen lines and a stir bar was placed 2-bromo-1-fluoro-3-methoxy-benzene (I-29, 2.0 g, 9.75 mmol) and dichloromethane (48 mL). The solution was cooled in an ice water bath for 15 minutes and then titanium tetrachloride (5.02 mL, 45.8 mmol) and dichloromethyl methyl ether (1.32 mL, 14.6 mmol) were added and the reaction mixture was allowed to warm to room temperature and react for 2 hours. The reaction mixture was slowly added to ice water (250 mL) and extracted with dichloromethane (2×100 mL). The organic portions were combined, washed with a saturated sodium bicarbonate solution (75 mL), water (75 mL) and brine (75 mL), dried (MgSO4) and concentrated. The crude material was triturated with hexanes (15 mL) to produce 1.67 g of 3-bromo-2-fluoro-4-methoxy-benzaldehyde (I-30) as an off-white solid in 74% yield. MS (ESI+): 233.2 (M+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791267B2
Source datasetuspto-grants-2014_07
ORD IDord-3036185e85674ea3bc8190418d6ed12d
Source noteuspto-grants-2014_07