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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2100250Generated: November 3, 2026

Ethyl Acetate → 1,1-dibromo-1,2-difluoro-2-(3-nitro-4-methoxy-phenyl)ethane

https://huagongshe.com/reaction/2100250

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant(Diethylamino)sulfur trifluorideHCID 123472—
ReactantHCID 12135311HCID 12135311—
SolventDichloromethaneHCID 6344—
Product1,1-dibromo-1,2-difluoro-2-(3-nitro-4-methoxy-phenyl)ethaneHCID 12135312—

Reaction Conditions

Temperature0 °C

Reaction Steps

(DAST 730 μL (5.58 mmol; 1.8 eq) in 5 mL CH2Cl2 was added to a solution of 1.146 g (3.1 mmol) of the alcohol (7) in 7 mL CH2Cl2 at −78° C. The reaction mixture was allowed to warm up to 0° C. over a period of 2 h, quenched with 15 mL of NaHCO3 saturated solution and diluted with 20 mL of diethyl ether. The organic phase was dried over anhydrous sodium sulfate and purified by chromatography on SiO2 using Hexane/Ethyl Acetate 7:3 to give 960 mg (2.6 mmol; 84%) of a yellow oil. Rf=0.493 (Hex./AcOEt 7:3)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572778B2
Source datasetuspto-grants-2009_08
ORD IDord-19ec94e11f5141bfb3c85a810b89c8da
Source noteuspto-grants-2009_08