HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1992846Generated: October 30, 2026
1,2-Epoxybutane → 1-(3-Methoxyphenyl)butan-2-ol
https://huagongshe.com/reaction/1992846
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,2-Epoxybutane | HCID 7834 | — |
| Reactant | HCID 178490745 | HCID 178490745 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(3-Methoxyphenyl)butan-2-ol | HCID 61261423 | 94% |
Reaction Steps
To a stirred suspension of CuI (0.40 g, 2.08 mmol) in 3-methoxyphenylmagnesium bromide in THF (31.2 mL, 1.0M THF solution, 31.2 mmol) at −20° C. was slowly added a solution of 1,2-epoxybutane (1.50 g, 20.8 mmol) in THF (1 mL). The mixture was allowed to warm up to room temperature and stirred at room temperature overnight. The reaction mixture was cooled in an ice bath and quenched with saturated aqueous NH4Cl. The mixture was extracted with ethyl acetate (3×70 mL). The combined organic phase was washed with 1 N NaOH, brine, dried (Na2SO4) filtered, and the filtrate was concentrated to give the crude product as a brown oil. The crude product was purified by flash chromatography over SiO2 with hexanes:EtOAc (4:1) to give 3.50 g (94%) of compound (51) as a colorless oil. 1H NMR (400 MHz, CDCl3): δ 1.00 (t, J=7.4 Hz, 3H), 1.50-1.65 (m, 2H), 2.62 (dd, J1=13.5 Hz, J2=8.6 Hz, 1H), 2.82 (dd, J1=13.5 Hz, J2=4.1 Hz, 1H), 3.74-3.79 (m, 1H), 3.80 (s, 3H), 6.75-6.85 (m, 3H), 7.20-7.25 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07649093B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-72921622dd57412d84de5fbed3b7e392 |
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| Source note | uspto-grants-2010_01 |
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