Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1,5-Pentanediol | HCID 8105 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-(Chloromethoxy)-2-methoxyethane | HCID 77590 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 15097256 | HCID 15097256 | 52.4% |
Reaction Steps
A solution of 50.00 g of 1,5-pentanediol dissolved in 100 ml of dimethylformamide was added dropwise to a mixture of 23.00 g of sodium hydride (as a 55% w/w dispersion in mine al oil) in 300 ml of dimethylformamide, whilst ice-cooling at 5° to 7° C. The mixture was stirred at room temperature for one hour, after which 65.79 g of 2-methoxyethoxymethyl chloride dissolved in 100 ml of dimethylformamide were added dropwise, whilst ice-cooling at 5° to 7° C. The mixture was stirred at room temperature for 3 hours, after which it was poured into 2.5 liters of water and then extracted five times with methylene chloride. The combined extracts were washed with water, dried and concentrated by evaporation under reduced pressure. The residue was subjected to column chromatography through 850 g of silica gel and 48.40 g of the title compound were obtained from the fractions eluted with a mixtures of methylene chloride and methanol ranging from 98:2 to 95:5 by volume, as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05068340 |
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| Source dataset | uspto-grants-1991_11 |
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| ORD ID | ord-c54d2588583f467da9978cd5788bccf2 |
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| Source note | uspto-grants-1991_11 |
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