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
Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Diiodobenzene | HCID 12208 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4-Benzyloxy-alpha-ethyldesoxybenzoin | HCID 18976513 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(4-Benzyloxy-phenyl)-1-(4-iodophenyl)-2-phenyl-butan-1-ol | HCID 18976457 | 108.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05807899 |
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| Source dataset | uspto-grants-1998_09 |
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| ORD ID | ord-ebe11cd1f0354c55aa6b82c1043a222f |
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| Source note | uspto-grants-1998_09 |
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