Formaldehyde → HCID 15728720, compound

HRID 654958Notes

Reaction equation

HRID 654958 reaction equation
[CH2:1]([SnH:5]([CH2:10][CH2:11][CH2:12][CH3:13])[CH2:6][CH2:7][CH2:8][CH3:9])[CH2:2][CH2:3][CH3:4].C([N-]C(C)C)(C)C.[Li+].[CH2:22]=[O:23].[CH3:24][O:25][CH2:26][CH2:27][O:28][CH2:29]Cl>C1CCCCC1.O1CCCC1>[CH2:10]([Sn:5]([CH2:22][O:23][CH2:29][O:28][CH2:27][CH2:26][O:25][CH3:24])([CH2:1][CH2:2][CH2:3][CH3:4])[CH2:6][CH2:7][CH2:8][CH3:9])[CH2:11][CH2:12][CH3:13]

Participants

7

Procedure

Tributyltin hydride (2.69 ml, 0.01 mol) was added dropwise to a solution of lithium diisopropylamide (a 1.5M solution in cyclohexane; 6.7 ml, 0.01 mol) in tetrahydrofuran (20 ml) at 0° under argon. After 15 minutes, paraformaldehyde (300 mg, 0.01 mol) was added, followed by 2-methoxyethoxymethyl chloride (1.15 ml, 0.01 mol) after 3 hours. Stirring was continued at room temperature for 12 hours and the mixture was quenched with water. Extraction (ethyl ether) and evaporation of the dried (magnesium sulphate) extracts gave an oil, which was flash chromatographed on silica using 5% ethyl ether/petroleum ether. Fractions with Rf of about 0.24 on evaporation afforded the desired ether as a colorless oil.

Workup

  1. customat 0°
  2. waitwas continued at room temperature for 12 hours
  3. customthe mixture was quenched with water
  4. extractionExtraction (ethyl ether) and evaporation of the
  5. dry with materialdried (magnesium sulphate)
  6. customextracts gave an oil, which
  7. customchromatographed on silica using 5% ethyl ether/petroleum ether
  8. customFractions with Rf of about 0.24 on evaporation
  9. customafforded the desired ether as a colorless oil

Sources & evidence

ORD record
ord-7917c03a1cc74c079caab00edb94767f
Source dataset
uspto-grants-1992_07
Patent number
US05134128

Reaction notes

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