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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | (Diethylamino)sulfur trifluoride | HCID 123472 | — |
| Reactant | HCID 12135311 | HCID 12135311 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1,1-dibromo-1,2-difluoro-2-(3-nitro-4-methoxy-phenyl)ethane | HCID 12135312 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07572778B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-19ec94e11f5141bfb3c85a810b89c8da |
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| Source note | uspto-grants-2009_08 |
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