Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromoeicosane | HCID 20271 | — |
| Reactant | 2H-Pyran, tetrahydro-2-(10-undecyn-1-yloxy)- | HCID 103566 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | Hexamethylphosphoramide | HCID 12679 | — |
| Product | HCID 15340538 | HCID 15340538 | 61.6% |
Reaction Steps
5 g (0.0198 mol) of 11-tetrahydropyranyloxyundecyne of Example 7 were placed in a mixture of 50 ml of THF and 25 ml of hexamethylphosphoric triamide under an argon atmosphere. At -60° C., 12.4 ml (0.0198 mol) of n-butyllithium in hexane were added dropwise. After 30 min at -60° C., a solution of 9.0 g (0.0248 mol) of 1-bromoeicosane in 25 ml of THF was added dropwise at -60° C. The mixture was left to warm up to room temperature. After 18 h at room temperature, it was poured into 25% aqueous NaH2PO4 solution and extracted with n-heptane (3×). The combined organic phases were dried (Na2SO4) and the solvent was removed. Flash chromatography on silica gel (n-heptane/ethyl acetate =15:1) gave 6.5 g (61.3% of theory) of 1-tetrahydropyranyloxy-hentriacont-10-yne.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05641767 |
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| Source dataset | uspto-grants-1997_06 |
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| ORD ID | ord-0fab22d819784f878b6e2afc57c65faa |
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| Source note | uspto-grants-1997_06 |
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