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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1270428Generated: October 25, 2026

Ammonium Chloride → 7-(Diphenylmethoxy)-1H-indole

https://huagongshe.com/reaction/1270428

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant1-(Benzhydryloxy)-2-nitrobenzeneHCID 7434122—
ReactantHCID 178418507HCID 178418507—
SolventTetrahydrofuranHCID 8028—
Product7-(Diphenylmethoxy)-1H-indoleHCID 15054008—

Reaction Steps

11.95 mmol of the compound obtained in Step A above are dissolved, under an inert atmosphere, in 80 ml of anhydrous tetrahydrofuran. The temperature of the reaction mixture is then lowered to −40° C. and then 41.84 mmol of a 1M solution of vinylmagnesium bromide in tetrahydrofuran are added dropwise to the solution, which is then stirred for 2 hours 50 minutes from −40° C. to 0° C. The reaction mixture is then hydrolysed at 0° C. using 100 ml of a saturated aqueous ammonium chloride solution, and the aqueous phase is extracted three times with ethyl acetate. The organic phases are combined, dried over magnesium sulphate, filtered and evaporated. Purification by flash chromatography over silica gel (petroleum ether/ethyl acetate: 9/1) allows the expected product to be isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07202255B2
Source datasetuspto-grants-2007_04
ORD IDord-ec4cca4f16c2406583ef840a41861f94
Source noteuspto-grants-2007_04