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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482184Generated: October 30, 2026

Hydrochloric Acid → Ethyl-12-(m-iodophenyl)-dodecanoate

https://huagongshe.com/reaction/482184

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIodineHCID 807—
ReactantEthyl-12-(m-aminophenyl)-dodecanoateHCID 14584161—
ReactantSodium NitriteHCID 23668193—
SolventAcetic AcidHCID 176—
SolventDiethyl EtherHCID 3283—
ProductEthyl-12-(m-iodophenyl)-dodecanoateHCID 14584162174.9%

Reaction Steps

Glacial acetic acid (4 ml) and concentrated HCl (2.5 ml) were added to a 50 ml Erlenmeyer flask containing ethyl-12-(m-amino-phenyl)-dodecanoate (3.92 g, 12.28 mmol). The mixture was cooled in a Nacl/ice bath. A cold aqueous solution of NaNO2 (4 ml, 3.1 M) was added to the mixture. The reaction was stirred for 40 minutes before a cold aqueous solution of KI/I2 (2.31/1.78 g, 7 ml) was added. The reaction mixture was allowed to warm to room temperature and was stirred overnight. Ether was added to the reaction mixture. The ether layer was separated and extracted with H2O, 10% Na2S2O3, H2O, sat. NaHCO3, and brine. The organic layer was dried (MgSO4) and the solvent removed under reduced pressure to give a reddish oil. The crude product was purified by column chromatography (120 g silica gel, hexanes:ethyl acetate 20:1) to yield a clear oil, compound 6, ethyl-12-(m-iodophenyl)-dodecanoate (5.28 g, 56.8% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05795561
Source datasetuspto-grants-1998_08
ORD IDord-c7c6b44c9035456ea49ea7b9b41ac8e7
Source noteuspto-grants-1998_08