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2-[(3-Bromophenyl)methoxy]oxane → 2-(3-Hydroxy-3-(3-((2-tetrahydropyranyloxy)methyl)phenyl)propyl)benzoic acid
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-[(3-Bromophenyl)methoxy]oxane | HCID 15282064 | — |
| 反応物 | 2-(3-Oxopropyl)benzoic acid | HCID 53938421 | — |
| 反応物 | HCID 178419628 | HCID 178419628 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 2-(3-Hydroxy-3-(3-((2-tetrahydropyranyloxy)methyl)phenyl)propyl)benzoic acid | HCID 54411298 | — |
反応手順
At -10° C., a solution of the aldehyde of Step 4 (5.045 g, 28.3 mmol) in 50 mL of THF was added dropwise to 0.57M 3-((2-tetrahydropyranyloxy)methyl)phenylmagnesium bromide in THF (120 mL, 68.4 mmol, prepared from the bromide of Step 2 and Mg in THF and filtered to remove the excess of Mg) and the mixture was stirred at r.t. for 30 min. At 0° C., 25% aq NH4OAc was added. The title product was extracted with EtOAc, dried over Na2SO4 and purified by flash chromatography on silica using acetone:toluene:HOAc 5:95:1 and 15:85:1.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05856322 |
| 出典データセット | uspto-grants-1999_01 |
| ORD ID | ord-bf60d37ce04a456caee9f7ddf358b70b |
| 出典メモ | uspto-grants-1999_01 |