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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 401548Generated: October 28, 2026

6-Bromo-2,2,4,4-tetrafluoro-1,3-benzodioxane → 2,2,4,4-tetrafluoro-4H-benzo[1,3]dioxine-6-carboxylic acid methyl ester

https://huagongshe.com/reaction/401548

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Bromo-2,2,4,4-tetrafluoro-1,3-benzodioxaneHCID 2773410—
CatalystHCID 178418397HCID 178418397—
SolventMethanolHCID 887—
SolventAcetonitrileHCID 6342—
SolventTriethylamineHCID 8471—
Product2,2,4,4-tetrafluoro-4H-benzo[1,3]dioxine-6-carboxylic acid methyl esterHCID 59166166169.8%

Reaction Conditions

Temperature75 °C

Reaction Steps

A suspension of 6-bromo-2,2,4,4-tetrafluoro-4H-benzo[1,3]dioxine (4.75 g, 16.6 mmol) and Pd(PPh3)4 (950 mg, 8.23 mmol) in MeOH (20 mL), MeCN (30 mL) and Et3N (10 mL) was stirred under carbon monoxide atmosphere (55 psi) at 75° C. (oil bath temperature) overnight. The cooled reaction mixture was filtered and the filtrate was concentrated. The residue was purified by silica gel column (Petroleum Ether) to give 2,2,4,4-tetrafluoro-4H-benzo[1,3]dioxine-6-carboxylic acid methyl ester (3.75 g, 85%). 1H NMR (CDCl3, 300 MHz) δ 8.34 (s, 1H), 8.26 (dd, J=2.1, 8.7 Hz, 1H), 7.22 (d, J=8.7 Hz, 1H), 3.96 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741933B2
Source datasetuspto-grants-2014_06
ORD IDord-927c15d7aaf2425bba98150dc6294594
Source noteuspto-grants-2014_06