Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 18960549 | HCID 18960549 | — |
| Reactant | HCID 178418689 | HCID 178418689 | — |
| Product | HCID 15661459 | HCID 15661459 | — |
Reaction Steps
1-(2-Tetrahydropyranyl)oxymethyl-3-(2-pyridyl)thiocarbonyl-9-fluorenone (470 mg) was dissolved in THF (10 ml) and cooled to -15° under N2. A solution of MeMgBr in THF (1.2 eq) was added dropwise over 5 min and the reaction allowed to stir at -10° C. for 0.5 hr. The reaction was quenched with saturated ammonium chloride solution, diluted with EtOAc, and washed with water, sat'd NaCl sol'n then dried and evaporated which gave a residue which was chromatographed on silica gel to give the product (233 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05356889 |
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| Source dataset | uspto-grants-1994_10 |
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| ORD ID | ord-6ccb7c667e9c4806a29f5e31aa125b03 |
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| Source note | uspto-grants-1994_10 |
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