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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 449780Generated: October 29, 2026

3-Chlorophenylacetic acid → HCID 22626651, compound

https://huagongshe.com/reaction/449780

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chlorophenylacetic acidHCID 15879—
ReactantN-bromobutanimideHCID 67184—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 22626651HCID 22626651—

Reaction Steps

3-Chlorophenylacetic acid (20.90 g, 122.51 mmol) and NBS (23.50 g, 132.03 mmol) were dissolved in carbon tetrachloride (300 mL), then BPO (300 mg) was added, the resulting reaction was heated to reflux under a sunlamp for 5 hours, then cooled to room temperature, filtered and concentrated to give the desired α-bromo-3-chlorophenylacetic acid. 1.40 g of this α-bromo-3-chlorophenylacetic acid was reacted with 3,4-dimethylphenol (686 mg) according to the General procedure C to give 1.47 g of the desired title compound. Spectroscopic data: 1H NMR (300 MHz, CDCl3) δ ppm 2.17 (s, 3 H) 2.21 (s, 3 H) 5.58 (s, 1 H) 6.65 (dd, J=8.20, 2.64 Hz, 1 H) 6.78 (d, J=2.64 Hz, 1 H) 7.01 (d, J=8.20 Hz, 1 H) 7.29-7.40 (m, 2 H) 7.42-7.52 (m, 1 H) 7.59 (s, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08486918B2
Source datasetuspto-grants-2013_07
ORD IDord-91140a1c438b4fd38f22a59b9ebdcc0e
Source noteuspto-grants-2013_07