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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2393586Generated: October 29, 2026

p-Diiodobenzene → 1-(4-Benzyloxy-phenyl)-1-(4-iodophenyl)-2-phenyl-butan-1-ol

https://huagongshe.com/reaction/2393586

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-DiiodobenzeneHCID 12208—
ReactantAmmonium ChlorideHCID 25517—
Reactant4-Benzyloxy-alpha-ethyldesoxybenzoinHCID 18976513—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product1-(4-Benzyloxy-phenyl)-1-(4-iodophenyl)-2-phenyl-butan-1-olHCID 18976457108.2%

Reaction Steps

A solution of 23.4 g of 1,4-diiodobenzene in 124 ml of tetrahydrofuran is mixed drop by drop at -70° C. under nitrogen with 45 ml of a 1.6 molar butyllithium solution, and it is stirred for 5 more minutes. Then, a solution of 18 g of 1-(4-benzyloxy-phenyl)-2-phenyl-butan-1-one [D. W. Robertson; J. A. Katzenellenbogen; D. J. Ellen; A. Rorke; B. S. Katzenellenbogen, J. Steroid Biochem., 1982, 16, 1-13] in 180 ml of tetrahydrofuran is added in drops, allowed to come to room temperature by completing the cooling, and it is stirred for 1 more hour. For working-up, 60 ml of saturated ammonium chloride solution is added, diluted with diethyl ether, washed neutral with water, dried on sodium sulfate, concentrated by evaporation in a vacuum and chromatographed on silica gel with pentane/diethyl ether. 31.5 g of 1-(4-benzyloxy-phenyl)-1-(4-iodophenyl)-2-phenyl-butan-1-ol is obtained as oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05807899
Source datasetuspto-grants-1998_09
ORD IDord-ebe11cd1f0354c55aa6b82c1043a222f
Source noteuspto-grants-1998_09