Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1,4-Butanediol | HCID 8064 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-(Octadecyloxy)propyl methanesulfonate | HCID 14719431 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 4-[3-(Octadecyloxy)propoxy]butanol | HCID 14719432 | — |
Reaction Steps
Sodium hydride (1.2 g) is heated at 70° C. for 10 minutes in dimethyl sulfoxide (50 ml), to which is added 1,4-butanediol (4.5 g). The mixture is heated for one further hour. To this reaction mixture is added dropwise a solution of 3-(octadecyloxy)propyl methanesulfonate obtained in Reference Example 1 (4.06 g) in dimethyl sulfoxide (15 ml), and the mixture is stirred at 70° C. for one hour. The reaction mixture is poured into cold water, and the mixture is subjected to extraction with a mixture of hexane and ethyl acetate. The extract is washed with water and then dried, and the solvents are then distilled off under reduced pressure. The residue is subjected to purification by means of silica gel column chromatography to obtain the above-titled compound (2.2 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05008454 |
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| Source dataset | uspto-grants-1991_04 |
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| ORD ID | ord-220cf47fe04b4b33a4de16b39a8fce54 |
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| Source note | uspto-grants-1991_04 |
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