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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803190Generated: November 2, 2026

(4-Chlorophenyl)acetic acid → 6-Chloro-2-(4-chlorophenyl)hexanoic acid

https://huagongshe.com/reaction/1803190

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Chlorophenyl)acetic acidHCID 15880—
Reactant1-Chloro-4-iodobutaneHCID 82527—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
Product6-Chloro-2-(4-chlorophenyl)hexanoic acidHCID 5811010990.7%

Reaction Steps

Step AH (1): 2-(4-Chlorophenyl)acetic acid (2.5 g, 14.65 mmol) was deprotonated with NaHMDS (1.0 M in THF, 29.3 mL, 29.3 mmol) and reacted with 1-chloro-4-iodobutane (1.80 mL, 14.7 mmol) using a procedure analogous to Step AC (1) to afford 6-chloro-2-(4-chlorophenyl)hexanoic acid (3.47 g, 59% yield). LC-MS (M−H)− 259.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349880B2
Source datasetuspto-grants-2013_01
ORD IDord-d30373d31e294df88d4716266f7eee27
Source noteuspto-grants-2013_01