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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803186Generated: November 2, 2026

1-Chloro-3-iodopropane → 2,4-Dichloro-α-(3-chloropropyl)benzeneacetic acid

https://huagongshe.com/reaction/1803186

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-3-iodopropaneHCID 81363—
Reactant2,4-Dichlorophenylacetic acidHCID 88209—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
Product2,4-Dichloro-α-(3-chloropropyl)benzeneacetic acidHCID 5811002558%

Reaction Steps

Step AD (1): 2-(2,4-Dichlorophenyl)acetic acid (10.25 g, 50.0 mmol) was deprotonated with NaHMDS (1.0 M in THF, 100 mL, 100 mmol) and reacted with 1-chloro-3-iodopropane (5.27 mL, 50.0 mmol) using a procedure analogous to Step AC (1) to afford, after purification by silica gel column chromatography, 5-chloro-2-(2,4-dichlorophenyl)pentanoic acid (8.15 g, 28.9 mmol, 58% yield) as a colorless oil. MS (M+H)+ 280.9. 1H NMR (500 MHz, chloroform-d) δ ppm 7.47 (d, J=2.14 Hz, 1 H) 7.34-7.40 (m, 1 H) 7.28-7.33 (m, 1 H) 4.22 (t, J=7.48 Hz, 1 H) 3.57 (t, J=6.41 Hz, 2 H) 2.27 (dddd, J=13.08, 10.64, 7.55, 5.34 Hz, 1 H) 1.95-2.05 (m, 1 H) 1.82-1.92 (m, 1 H) 1.68-1.81 (m, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349880B2
Source datasetuspto-grants-2013_01
ORD IDord-186ed9c412f14a7a996c348dcf88b55c
Source noteuspto-grants-2013_01