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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2420654Generated: November 2, 2026

Pentane → Butanoic acid, 3-[(4-methoxyphenyl)thio]-3-methyl-

https://huagongshe.com/reaction/2420654

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPentaneHCID 8003—
ReactantPiperidineHCID 8082—
Reactant3-Methyl-2-butenoic acidHCID 10931—
Reactant4-MethoxybenzenethiolHCID 12765—
SolventEthyl AcetateHCID 8857—
ProductButanoic acid, 3-[(4-methoxyphenyl)thio]-3-methyl-HCID 10171427—

Reaction Conditions

Temperature107.5 °C

Reaction Steps

A heavy-walled screw-cap tube was charged with 3-methyl-2-butenoic acid (13.86 gm) 3,3-dimethylacrylic acid, (138.4 mmol), 4-methoxythiophenol (143.2 mmol), and piperidine (41.6 mmol) [Aldrich]. The mixture was heated to 105-110° C. for 32 hours, then cooled to room temperature. The reaction mixture was dissolved in ethyl acetate (EtOAc) (700 ml) with stirring, and the resulting solution was washed with 1M aqueous HCl (50 ml×2), water (50 ml), and saturated aqueous NaCl (50 ml). The organic solution was thereafter dried over NaSO4. Concentration of this organic solution under reduced pressure afforded an oil and 2 days incubation at −20° C. yielded a crystalline solid. Forty ml of pentane were added to the solid, which was then crushed and filtered. The solid was washed on filter paper with pentane (20 ml, 2 times) to yield the product 3-(4-methoxyphenylthio)-3-methyl-butyric acid, as pale yellow crystals (31.4 grams, 94.4% yield, m.p. 62-64° C.), [1H-NMR(CDCl3): d7.5 (t, 2H, J=8 Hz), d6.9 (t, 2H, J=6.7 Hz), d3.9 (s, 3H, J=16.1 Hz), d2.6 (s, 2H), d1.3 (s, 6H)].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07955852B2
Source datasetuspto-grants-2011_06
ORD IDord-f2ae0542353b4fae841aca68c68e59a0
Source noteuspto-grants-2011_06