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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIodineHCID 807—
ReactantEthyl BromideHCID 6332—
ReactantMagnesiumHCID 5462224—
Reactant(r)-2-Phenyl-1-(4-chlorophenyl)propaneHCID 69111420—
SolventTetrahydrofuranHCID 8028—
Product(r)-2-Phenyl-1-(4-iodophenyl)propaneHCID 69111052100%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07108895B2
Source datasetuspto-grants-2006_09
ORD IDord-e45a4313e4b4493db2b4f8201aa1202d
Source noteuspto-grants-2006_09