HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2214320Generated: October 30, 2026
Hydrochloric Acid → (r)-2-Phenyl-1-(4-iodophenyl)propane
https://huagongshe.com/reaction/2214320
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Iodine | HCID 807 | — |
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | (r)-2-Phenyl-1-(4-chlorophenyl)propane | HCID 69111420 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (r)-2-Phenyl-1-(4-iodophenyl)propane | HCID 69111052 | 100% |
Reaction Steps
35 ml of tetrahydrofuran (THF) was added to 11.6 g (0.48 mol) of magnesium, and a solution having 23.6 g (0.22 mol) of ethyl bromide dissolved in 70 ml of THF was dropwise added thereto over a period of 1 hour at room temperature with stirring, followed by stirring for 1 hour. A solution having 50.0 g (0.22 mol) of (R)-2-phenyl-1-(4-chlorophenyl)propane dissolved in 50 ml of THF was dropwise added thereto over a period of 30 minutes at room temperature, followed by stirring under reflux for 5 hours. After the mixture was cooled to room temperature, 250 ml of THF was added thereto, and the mixture was further cooled to −30° C. A solution having 112 g (0.44 mol) of iodine dissolved in 300 ml of THF was dropwise added thereto at −30° C. over a period of 30 minutes, followed by stirring for 1 hour. The temperature was raised to 0° C., and 120 ml of 4M hydrochloric acid was dropwise added thereto, followed by stirring for 10 minutes. After extraction with toluene from the reaction liquid, washing with water and drying were carried out to obtain 69.8 g of (R)-2-phenyl-1-(4-iodophenyl)propane (GC purity: 95.2%, 0.22 mol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07108895B2 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-e45a4313e4b4493db2b4f8201aa1202d |
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| Source note | uspto-grants-2006_09 |
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