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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 576040Generated: October 25, 2026

Hydrochloric Acid → 1-Chloro-3-iodo-5-(trifluoromethyl)benzene

https://huagongshe.com/reaction/576040

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPhosphinic AcidHCID 4124402—
ReactantSodium NitriteHCID 23668193—
Reactant2-Chloro-6-iodo-4-(trifluoromethyl)anilineHCID 56587696—
SolventWaterHCID 962—
Product1-Chloro-3-iodo-5-(trifluoromethyl)benzeneHCID 1536595766%

Reaction Conditions

Temperature57.5 °C

Reaction Steps

2-Chloro-6-iodo-4-(trifluoromethyl)benzenamine (i.e. the product of Example 4) (31.8 g, 98.9 mmol) was added to hydrochloric acid (36%, 190 mL) and the mixture was warmed to 55-60° C. for 20 min. The mixture was cooled to 0° C. Sodium nitrite (13.6 g, 197 mmol) in water (36 mL) was added over 30 min. When the addition was complete the mixture was stirred at 0-5° C. for 70 min. Hypophosphorous acid (50%, 36.5 mL, 351 mmol) was added dropwise at 5-10° C. over 40 min. When the addition was complete the mixture spontaneously warmed briefly to 35° C., and was then cooled to 10-20° C. After stirring at 10-20° C. for 2 h, the mixture was stored in a refrigerator overnight. Then the mixture was warmed to room temperature and was stirred for 1 h. The mixture was diluted with water (400 mL) and extracted with ether (2×250 mL). The combined extracts were dried and evaporated. Distillation gave the product as an oil (19.93 g, 66% yield), b.p. 98-112° C. at 2.0 kPa.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09035101B2
Source datasetuspto-grants-2015_05
ORD IDord-7e8a47bf4116403885a546c46911c778
Source noteuspto-grants-2015_05