HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1751835Generated: October 28, 2026
Hexane → 4-(3-Oxobutyl)benzoic acid methyl ester
https://huagongshe.com/reaction/1751835
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | 3-Buten-2-ol | HCID 11716 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Methyl 4-bromobenzoate | HCID 12081 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-(3-Oxobutyl)benzoic acid methyl ester | HCID 10932640 | 26.1% |
Reaction Steps
To a solution of methyl-4-bromobenzoate (1.0 g, 4.65 mmol) in triethylamine (13 mL) was added 3-buten-2-ol (1 mL, 11.63 mmol), palladium (II) acetate (0.104 g, 0.465 mmol), and then triphenylphosphine (0.244 g, 0.93 mmol). The reaction was stirred in a 75° C. oil bath overnight under nitrogen atmosphere. Monitoring by TLC (3:1 hexane:ethyl acetate) showed the product and aryl bromide. The reaction was cooled to room temperature and then concentrated. Water was then added followed by extraction with ethyl acetate. The organic layer was washed with water and brine, dried over Na2SO4, filtered and concentrated. The crude product was purified by flash column chromatography (5:1 to 3:1 hexane:ethyl acetate) to obtain the product (250 mg, 26% yield). 1H NMR (600 MHz, CDCl3): δ 7.95 (d, 2H, J=8.4 Hz), 7.25 (d, 2H, J=8.4 Hz), 3.90 (s, 3H), 2.95 (t, 2H, J=7.45 Hz), 2.77 (t, 2H, J=7.68 Hz), 2.14 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09161997B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-431d31c9758d470abb88627a12c5c45f |
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| Source note | uspto-grants-2015_10 |
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