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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1742728Generated: October 31, 2026

Tetrahydrofuran → HCID 86748088, compound

https://huagongshe.com/reaction/1742728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 19007818HCID 19007818—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
ProductHCID 86748088HCID 8674808863.2%

Reaction Steps

Into a similar reaction vessel, as used in the abovementioned reaction, were placed 1.342 parts of t-BuOK and 7.607 parts of THF and to this, a mixture of 10.000 parts of 1propargyloxybiphenyl and 23.333 parts of THF was added dropwise. The content was reacted at 50° C. for 60 minutes and then a deionized water was added to stop the reaction. THF layer and water layer were removed by using an evaporator, and the residue was subjected to a column chromatography (silica gel 200 mesh) to obtain a purified 1-allenyloxy biphenyl as colorless oily product. This compound was identified by FT-NMR(H) and IR spectrum. The reaction yield was 63.2%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05340931
Source datasetuspto-grants-1994_08
ORD IDord-9cd0d69b6d5d461aba91f998fdac4389
Source noteuspto-grants-1994_08