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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1110432Generated: November 2, 2026

2-Nitrophenol → 2,2-Dimethyl-5-(3-nitrophenoxy)pentanoic acid, methyl ester

https://huagongshe.com/reaction/1110432

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-NitrophenolHCID 6947—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 5-bromo-2,2-dimethylpentanoateHCID 13050502—
SolventAcetonitrileHCID 6342—
Product2,2-Dimethyl-5-(3-nitrophenoxy)pentanoic acid, methyl esterHCID 13171619894%

Reaction Steps

A mixture of 27.8 g (200 mmol) of 2-nitrophenol, 44.6 g (200 mmol) of methyl-5-bromo-2,2-dimethylpentanoate (Journal of Medicinal Chemistry, Vol. 26, pp 1020-1027 (1983)) and 30.5 g (220 mmol) of anhydrous potassium carbonate in 300 ml of acetonitrile is stirred at reflux for 18 hours. The inorganic salts are removed, washed with acetonitrile and the filtrate is concentrated on a rotary evaporator. The residue is taken up in diethyl ether and the solution washed with 2N potassium hydroxide (3×50 ml), brine, dried (magnesium sulfate), and evaporated to afford 55.9 g of crude product. Distillation gives 52.9 g of 2,2-dimethyl-5-(3-nitrophenoxy)pentanoic acid, methyl ester, bp 160°-165° C. (0.5 mm).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04975456
Source datasetuspto-grants-1990_12
ORD IDord-dec8f9896dba4ad08c77bf610d1e669f
Source noteuspto-grants-1990_12