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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 346838Generated: October 25, 2026

2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → 1,1,1,3,3,3-hexafluoro-2-[1-(2-hydroxy-1-phenyl-ethyl)-2-methyl-1H-indol-5-yl]-propan-2-ol

https://huagongshe.com/reaction/346838

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
ReactantAmmonium ChlorideHCID 25517—
Reactant1,4-DioxaneHCID 31275—
Reactant1,1,1,3,3,3-hexafluoro-2-[1-(2-hydroxy-1-phenyl-ethyl)-2-methyl-2,3-dihydro-1H-indol-5-yl]-propan-2-olHCID 11509976—
CatalystManganese dioxideHCID 14801—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
Product1,1,1,3,3,3-hexafluoro-2-[1-(2-hydroxy-1-phenyl-ethyl)-2-methyl-1H-indol-5-yl]-propan-2-olHCID 1166885038.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 40 mg (0.094 mmol) 1,1,1,3,3,3-hexafluoro-2-[1-(2-hydroxy-1-phenyl-ethyl)-2-methyl-2,3-dihydro-1H-indol-5-yl]-propan-2-ol (example 70) in 1 mL of toluene was treated with 45 mg (0.47 mmol) of MnO2. After stirring at 80° C. for 8 hrs, 0.5 mL of dioxane and 22 mg (0.094 mmol) of DDQ were added. The resulting mixture was stirred at RT overnight and poured into a saturated aqueous solution of NH4Cl and Et2O. The phases were separated and the aqueous one was extracted with Et2O. The combined organic phases were dried over Na2SO4 and evaporated. Column chromatography on silica gel with n-heptane/EtOAc 2:1 yielded 15 mg (38%) of 1,1,1,3,3,3-hexafluoro-2-[1-(2-hydroxy-1-phenyl-ethyl)-2-methyl-1H-indol-5-yl]-propan-2-ol, brown oil, MS: 418 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07173048B2
Source datasetuspto-grants-2007_02
ORD IDord-54e30725d0064c92886c1a462bc25ce2
Source noteuspto-grants-2007_02