Methyl Ethyl Ketone → HCID 21912828, compound

HRID 1245580Notes

Reaction equation

HRID 1245580 reaction equation
[H-].[Na+].[CH3:3][C:4](=[O:7])[CH2:5][CH3:6].[Cl:8][CH2:9][CH2:10][CH2:11][CH2:12][C:13]([O:15]C)=O>C1COCC1>[Cl:8][CH2:9][CH2:10][CH2:11][CH2:12][C:13](=[O:15])[CH2:3][C:4](=[O:7])[CH2:5][CH3:6]

Participants

5

Conditions

Temperature
0 °C

Procedure

To a suspension of NaH (60% dispersion in mineral oil: 8.88 g) in THF (250 mL) was added a mixture of 2-butanone (7.98 g) and methyl 5-chlorovalerate (50.0 g) in THF (100 mL) dropwise via cannula at 0° C. The mixture was stirred at 0° C. for 10 min and at rt for 24 h. After the reaction was quenched with 2 N HCl (200 mL), aqueous layer was extracted with EtOAc (3×). Concentration of the combined organic phase gave a brown colored oil, which was purified by fractional vacuum distillation. The title compound was collected in the temperature range between 95° C. and 110° C. at 10 mmHg. 1H NMR (500 MHz, CDCl3) δ 1.14 (t, 3H, J=7.4 Hz), 1.65–1.90 (m, 4H), 2.30–2.60 (m, 4H), 3.50–3.60 (m, 2H), 5.51 (s, 1H).

Workup

  1. additionwas added
  2. customAfter the reaction was quenched with 2 N HCl (200 mL), aqueous layer
  3. extractionwas extracted with EtOAc (3×)
  4. customConcentration of the combined organic phase gave a brown colored oil, which
  5. distillationwas purified by fractional vacuum distillation
  6. customThe title compound was collected in the temperature
  7. customrange between 95° C. and 110° C. at 10 mmHg

Sources & evidence

ORD record
ord-f27202bbab6a4a56bae1300f871db4d6
Source dataset
uspto-grants-2006_10
Patent number
US07125887B2

Reaction notes

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