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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1866157Generated: November 2, 2026

Iodine → HCID 13981859, compound

https://huagongshe.com/reaction/1866157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSulfuric AcidHCID 1118—
Reactant2,2,2-Trifluoro-N-[(2R)-1-phenylpropan-2-yl]acetamideHCID 14877236—
ReactantHCID 86590690HCID 86590690—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductHCID 13981859HCID 13981859185.4%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 2,2,2-trifluoro-N-[(1R)-1-methyl-2-phenylethyl]acetamide (3.75 g) in acetic acid (32 ml)—water (6.5 ml)—sulfuric acid (0.97 ml) were added iodine (1.65 g) and periodic acid dihydrate (740 mg) at room temperature, and the mixture was heated to 60-80° C. for 5 hours. After being allowed to cool to room temperature, the mixture was partitioned between hexane/ethyl acetate and water. The organic layer was separated, washed successively with water, sodium sulfite solution, water and brine, dried over magnesium sulfate, and filtered. The filtrate was concentrated and the residue was recrystallized from diisopropyl ether (44 ml) to give 2,2,2-trifluoro-N-[(1R)-2-(4-iodophenyl)-1-methylethyl]acetamide (2.15 g) as a colorless needle.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07629366B2
Source datasetuspto-grants-2009_12
ORD IDord-e6524968bccc4ad7869092a7003e6b7b
Source noteuspto-grants-2009_12