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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253303Generated: October 30, 2026

Triethylamine → 7-(Chloromethyl)-5-fluoro-2,3-dihydro-1,4-benzodioxine

https://huagongshe.com/reaction/253303

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantThionyl ChlorideHCID 24386—
Reactant(8-Fluoro-2,3-dihydro-1,4-benzodioxin-6-yl)methanolHCID 66891073—
SolventDichloromethaneHCID 6344—
Product7-(Chloromethyl)-5-fluoro-2,3-dihydro-1,4-benzodioxineHCID 6688939899.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of (8-fluoro-2,3-dihydro-1,4-benzodioxin-6-yl)methanol (0.84 g, 4.55 mmol) and triethylamine (960 μl, 4.84 mmol) in dichloromethane (20 mL) was slowly added thionyl chloride (400 μl, 5.47 mmol) at 0° C. The solution was stirred at 0° C. for 15 min then at rt for 3 h. Dichloromethane (80 mL) was added and the solution was washed with water (40 mL), saturated aqueous sodium bicarbonate (40 mL) then brine (40 mL) and dried over sodium sulfate. Filtration and concentration gave 7-(chloromethyl)-5-fluoro-2,3-dihydro-1,4-benzodioxine (0.92 g, quantitative yield) as a brown oil. The chloride was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07872014B2
Source datasetuspto-grants-2011_01
ORD IDord-a09af8cc166b4f4b96e94c5d17242f8f
Source noteuspto-grants-2011_01