Methyl iodide → HCID 86590997, compound

HRID 2416416Notes

Reaction equation

HRID 2416416 reaction equation
[Cl:1][CH2:2][CH2:3][CH2:4][CH2:5][C@H:6]([OH:8])[CH3:7].[C:9](=O)([O-])[O-].[K+].[K+].IC.[H-].[Na+]>O.CN(C)C=O>[Cl:1][CH2:2][CH2:3][CH2:4][CH2:5][C@H:6]([O:8][CH3:9])[CH3:7]

Participants

7

Conditions

Temperature
40 °C

Procedure

A mixture of (R)-1-chloro-5-hydroxyhexane, dimethylformamide (100 ml), powdered potassium carbonate (1 g), iodomethane (15.9 g, 112 mmol) and sodium hydride (2.0 g, 84 mmol) were combined was heated at 40° C. for 30 minutes. After cooling to room temperature, water (100 ml) was added cautiously and the mixture was extracted with hexanes (2×100 ml). The combined extracts were concentrated under vacuum and the residue was purified by column chromatography on silica gel eluting with hexanes followed by 10% ethyl acetate-hexanes to afford (R)-1-chloro-5-methoxyhexane (3.1 g, 43% yield for 2 steps) as a clear oil. 1H NMR (300 MHz, CDCl3) δ 1.15 (d, 3H), 1.36-1.56 (m, 4H), 1.70-1.84 (m, 2H), 3.28 (s, 3H), 3.29 (m, 1H), 3.52 (t, 2H).

Workup

  1. temperatureAfter cooling to room temperature
  2. extractionthe mixture was extracted with hexanes (2×100 ml)
  3. concentrationThe combined extracts were concentrated under vacuum
  4. customthe residue was purified by column chromatography on silica gel eluting with hexanes

Sources & evidence

ORD record
ord-fa00f4ddba23442a80f28487dce969ed
Source dataset
uspto-grants-2004_11
Patent number
US06825180B2

Reaction notes

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