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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pentane | HCID 8003 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 3-Methyl-2-butenoic acid | HCID 10931 | — |
| Reactant | 4-Methoxybenzenethiol | HCID 12765 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Butanoic acid, 3-[(4-methoxyphenyl)thio]-3-methyl- | HCID 10171427 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07955852B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-f2ae0542353b4fae841aca68c68e59a0 |
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| Source note | uspto-grants-2011_06 |
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