Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2-Methoxyethanol | HCID 8019 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-(3-Chloromethylphenoxymethyl)quinoline hydrochloride | HCID 14501707 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20037837 | HCID 20037837 | — |
Reaction Steps
1.1 g (0.015 mol) of 2-methoxyethanol was dissolved in 50 ml THF. To this solution 1.5 g (0.03 mol, 50% oil dispersion) NaH, (0.015 mol) 2-(3-chloromethylphenoxymethyl)quinoline hydrochloride, was added slowly. After the addition was completed, the mixture was heated at 70° C. bath temperature for overnight. The reaction mixture was poured into water and extracted with ether. The ether extract was washed with water, dried and concentrated to dryness under reduced pressure. The residue was passed through a silica gel column using hexane/ethylacetate (3:1) as eluent. Evaporation of eluent gave light yellow oil (1.1 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04839369 |
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| Source dataset | uspto-grants-1989_06 |
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| ORD ID | ord-b9ba34ccf7c04b23a779a6c48ed3e79d |
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| Source note | uspto-grants-1989_06 |
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