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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 589345Generated: October 30, 2026

2-Iodoaniline → (2-Iodophenyl)hydrazine

https://huagongshe.com/reaction/589345

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-IodoanilineHCID 11995—
ReactantStannous chloride dihydrateHCID 61436—
ReactantSodium NitriteHCID 23668193—
SolventHydrochloric AcidHCID 313—
Product(2-Iodophenyl)hydrazineHCID 138194144%

Reaction Conditions

Temperature0 °C

Reaction Steps

21.9 g (100 mmol) o-iodophenyl amine was dissolved in 40 mL concentrated hydrochloric acid. At 0° C., 6.9 g (100 mmol) sodium nitrite (dissolved in 35 mL water) was added dropwise, and stirred at 0° C. for half an hour. Then, SnCl2.2H2O 64.7 g (300 mmol) (dissolved in 70 mL concentrated hydrochloric acid) was added dropwise slowly, and reacted for about 3 h until complete. It was filtered to obtain a white solid, washed with a saturated solution of sodium chloride, and then washed with a mixed solvent of petroleum ether and diethyl ether (1:1). Then, the solid was adjusted to be basic with sodium hydroxide solution. The solid impurity therein was filtered, the aqueous phase was extracted with dichloromethane several times, the organic phases combined, dried, rotate evaporated to dryness to obtain a colorless oil 10.3 g, at a yield of 44.0%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09233098B2
Source datasetuspto-grants-2016_01
ORD IDord-ba65a172163c42eb8567bf2271d00387
Source noteuspto-grants-2016_01