Dibromomethane → (Z)-2-(4-Phenylbut-3-enyl)oxirane

HRID 1295077Notes

Reaction equation

[C:1]1(/[CH:7]=[CH:8]\[CH2:9][CH2:10][CH:11]=[O:12])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.Br[CH2:14]Br.[NH4+].[Cl-]>C1COCC1>[C:1]1(/[CH:7]=[CH:8]\[CH2:9][CH2:10][CH:11]2[CH2:14][O:12]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

Participants

Conditions

Temperature: -78 °C

Procedure

(Z)-5-Phenylpent-4-enal (0.475 g, 2.97 mmol) and dibromomethane (0.626 g, 3.60 mmol) were taken up in THF (20 mL) and chilled to −78° C. under argon n-butyl lithium (1.6M in hexane, 2.0 mL, 3.20 mmol) was added dropwise over 5 minutes. The resulting mixture was warmed slowly to room temperature and stirred overnight. The reaction mixture was poured into saturated aqueous NH4Cl (20 mL), extracted with MTBE (2×30 mL) and solvent removed under reduced pressure. The resulting oil was purified by column chromatography (0–20% EtOAc/n-hexane, silica) to give (Z)-2-(4-Phenylbut-3-enyl)oxirane as a pale yellow oil. 1H NMR (CDCl3): δ 7.32–7.27 (m, 2H), 7.25–7.19 (m, 3H), 6.47 (d, 1H, J=11.7), 5.68 (J1=11.6, J2=7.3), 2.97–2.93 (m, 1H), 2.77–2.74 (m, 1H), 2.55–2.52 (m, 1H), 2.53–2.48 (m, 2H), 1.76–1.67 (m, 2H). Contains ca. 18% (E)-2-4-phenylbut-3-enyl)oxirane.

Workup

additionwas added dropwise over 5 minutes
temperatureThe resulting mixture was warmed slowly to room temperature
extractionextracted with MTBE (2×30 mL) and solvent
customremoved under reduced pressure
customThe resulting oil was purified by column chromatography (0–20% EtOAc/n-hexane, silica)

Sources & evidence

ORD record: ord-57a18c7c7277477d8a3279451d3f0405
Source dataset: uspto-grants-2007_07
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07241792B2

Reaction notes

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