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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 633438Generated: October 30, 2026

1,2-Difluoro-4-nitrobenzene → HCID 58377132, compound

https://huagongshe.com/reaction/633438

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-Difluoro-4-nitrobenzeneHCID 123053—
Reactant2-(tert-Butyl(dimethyl)silyl)oxyethanolHCID 11137665—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58377132HCID 58377132102.1%

Reaction Steps

The same procedure detailed below for Compound 133 was used, but using 3,4-difluoronitrobenzene (225 mg, 1.4 mmol), potassium tert-butoxide (354 mg, 3.2 mmol) and 2-((tert-butyldimethylsilyl)oxy)ethan-1-ol (506 mg, 2.9 mmol) in THF (3 mL) to give the product (451 mg) after workup (yield assumed quantitative). The product was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321763B2
Source datasetuspto-grants-2016_04
ORD IDord-8e84b5f8cbe34142baeebc868d6f800e
Source noteuspto-grants-2016_04