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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588881Generated: November 4, 2026

2-Amino-5-chloro-4-iodophenol → HCID 117607191, compound

https://huagongshe.com/reaction/588881

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-5-chloro-4-iodophenolHCID 92135481—
ReactantHCID 178418630HCID 178418630—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventTetrahydrofuranHCID 8028—
ProductHCID 117607191HCID 11760719163.1%

Reaction Steps

To a mixture of 2-amino-5-chloro-4-iodophenol (500 mg, 1.9 mmol), PdCl2(dppf) (136 mg, 0.19 mmol) in THF (10 mL) under argon at RT, cyclopropylmagnesium bromide (16 mL, 11.4 mmol, 0.7 M in THF) was added and the mixture was stirred at reflux for 15 h. The mixture was allowed to cool to RT, and partitioned between ethyl acetate and water. The organic layer was washed with brine, dried over Na2SO4 and concentrated. The residue was purified by flash column chromatography on silica gel (10-20% ethyl acetate/hexanes) to afford the desired product (220 mg, 63% yield) as a brown solid. 1H NMR (400 MHz, DMSO-d6) δ: 9.27 (s, 1H), 6.62 (s, 1H), 6.22 (s, 1H), 4.53 (s, 2H), 1.89-1.93 (m, 1H), 0.83-0.87 (m, 2H), 0.46-0.49 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227978B2
Source datasetuspto-grants-2016_01
ORD IDord-605e8c3cc6774f50aaa91981b553ad1b
Source noteuspto-grants-2016_01