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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 592353Generated: October 30, 2026

Hydrochloric Acid → 2-(2-Iodophenyl)propanamide

https://huagongshe.com/reaction/592353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
ReactantAmmonium CarbonateHCID 517111—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant2-(2-Iodophenyl)propanoic acidHCID 22236851—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product2-(2-Iodophenyl)propanamideHCID 86712277—

Reaction Steps

A solution of 2-(2-iodophenyl)propanoic acid (9.73 g, 35.2 mmol) in THF (24 mL), DMF (4 mL) and DIPEA (30.7 mL, 0.176 mol) was stirred with HOBt (7.14 g, 52.9 mmol) and EDCl.HCl (10.1 g, 52.9 mmol) for 10 minutes at room temperature under N2. Ammonium carbonate (16.9 g, 0.176 mol) was then added and the reaction mixture was stirred overnight at room temperature. The volatiles were removed under reduced pressure before sat. aq. NaHCO3 (100 mL) was added to the residue. The aqueous phase was extracted with EtOAc (3×100 mL) and the combined organics were washed with brine, dried over MgSO4 and the volatiles were removed in vacuo to give the impure title compound I13 as a pale yellow solid (˜95% purity, 10.05 g, >95%). LCMS-D: rt 3.12 min; m/z 276 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238644B2
Source datasetuspto-grants-2016_01
ORD IDord-c331bba519b8463eaa897cac4789a061
Source noteuspto-grants-2016_01