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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 627451Generated: October 29, 2026

Triethylsilane → (1,1'-Biphenyl)-2-ol

https://huagongshe.com/reaction/627451

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylsilaneHCID 12052—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 86714195HCID 86714195—
SolventTolueneHCID 1140—
Product(1,1'-Biphenyl)-2-olHCID 701735%
Product3-(Triethylsilyl)biphenyl-2-olHCID 8671419326%
Product2-(3-Triethylsilylphenyl)phenolHCID 8671419412%

Reaction Steps

The reaction was conducted according to the General Procedure by heating 4-Et3Si-dibenzofuran (3, 141 mg, 0.5 mmol, 1 equiv.), KOt-Bu (112 mg, 1 mmol, 2 equiv.) and Et3SiH (401 microliters, 2.5 mmol, 5 equiv.) in 2 ml of toluene for 20 hours at 100° C. After acidic aqueous work up, the crude reaction mixture was purified by chromatography on silica using hexanes and hexanes-ether (10:1) to isolate 2-phenylphenol (2, 30 mg, 0.177 mmol, 35%), 2-triethylsilyl-6-phenylphenol (5, 37 mg, 0.134 mmol, 26%), 2-(3-triethylsilylphenyl)phenol (6, 17 mg, 0.063 mmol, 12%). Quantities of unconsumed 3 as well as products 1, 4 and 7 were obtained using post-chromatography GC-FID analysis of the corresponding mixed fractions.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309269B2
Source datasetuspto-grants-2016_04
ORD IDord-e7baaa019cd2441a84a34c9d994aa045
Source noteuspto-grants-2016_04