HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1270428Generated: October 25, 2026
Ammonium Chloride → 7-(Diphenylmethoxy)-1H-indole
https://huagongshe.com/reaction/1270428
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1-(Benzhydryloxy)-2-nitrobenzene | HCID 7434122 | — |
| Reactant | HCID 178418507 | HCID 178418507 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 7-(Diphenylmethoxy)-1H-indole | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07202255B2 |
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| Source dataset | uspto-grants-2007_04 |
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| ORD ID | ord-ec4cca4f16c2406583ef840a41861f94 |
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| Source note | uspto-grants-2007_04 |
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