HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 858780Generated: October 25, 2026
1-Cyclopentyl-2-propen-1-ol → HCID 68866580, compound
https://huagongshe.com/reaction/858780
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Cyclopentyl-2-propen-1-ol | HCID 145133 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 43084322 | HCID 43084322 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 68866580 | HCID 68866580 | 93% |
Reaction Steps
A mixture of (4-bromo-2-fluorophenoxy)acetonitrile (2.5 g, 10.8 mmol), 1-Cyclopentyl-2-propen-1-ol (2.0 g, 16.2 mmol), dichlorobis (triphenylphosphine) palladium (II) (151 mg, 0.22 mmol), and sodium bicarbonate (1.08 g, 12.9 mmol) in N-methylpyrrolidinone (20 mL) was heated to 140° C. under N2 for 5 hours. The reaction mixture was partitioned between 1N HCl and EtOAc. The organic layer was washed with saturated NaHCO3, brine, dried over Na2SO4 and concentrated to a black oil. The oil was purified by flash column chromatography (Hexanes to 10% EtOAc in hexanes) to give the desired product (2.7 g, 93%). 1H NMR (CDCl3): δ 1.52–1.83 (m, 8H), 2.75 (m, 2H), 2.85 (m, 3H), 4.80 (s, 2H), 6.92–7.06 (m, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07148226B2 |
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| Source dataset | uspto-grants-2006_12 |
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| ORD ID | ord-8834134a3af544e1878df7d64b6e2710 |
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| Source note | uspto-grants-2006_12 |
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