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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241436Generated: November 1, 2026

Diethyl Ether → HCID 67970696, compound

https://huagongshe.com/reaction/241436

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantTriethylamineHCID 8471—
Reactant1,3-Bis(diphenylphosphino)propaneHCID 81219—
ReactantHCID 67970619HCID 67970619—
ReactantHCID 178418416HCID 178418416—
Catalystpalladium(II) acetateHCID 167845—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
ProductHCID 67970696HCID 6797069677%

Reaction Steps

Purge a mixture of 3-bromo-4-(difluoromethyl)benzonitrile (8.87 g, 38.2 mmol, 1.0 equiv), triethylamine (16.0 mL, 114.7 mmol, 3.0 equiv), MeOH (70 mL), and DMF (120 mL) with nitrogen; then treat the mixture with palladium(II) acetate (867 mg, 3.82 mmol, 0.1 equiv) and 1,3-bis(diphenylphosphino)propane (1.61 g, 3.82 mmol, 0.1 equiv). Stir the mixture under 138 kPag of carbon monoxide at room temperature for two days and then 80° C. for one day. Cool the mixture to room temperature, and dilute with Et2O (300 mL). Wash the mixture with water and saturated sodium chloride, and separate the organic layer. Dry the organic layer over sodium sulfate; filter; collect the filtrate; and concentrate under reduced pressure. Subject the resulting crude material to silica gel chromatography eluting with a gradient of 10-15% THF/hexanes gradient to give the title compound (6.19 g, 77% yield). ES/MS (m/z) 211 (M).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08648200B2
Source datasetuspto-grants-2014_02
ORD IDord-5f5bb4786d9242949fde6abeaade1c95
Source noteuspto-grants-2014_02