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Tetrahydrofuran → (S)-2-{2[2-(1-methoxycarbonylethoxy)phenyl]vinyl}-1-methylindole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | Triphenylphosphine | HCID 11776 | — |
| 反応物 | Diethyl azodicarboxylate | HCID 5462977 | — |
| 反応物 | 2-[2-(2-Hydroxyphenyl)vinyl]-1-methylindole | HCID 69955635 | — |
| 溶媒 | Sodium chloride; water | HCID 57417360 | — |
| 生成物 | (S)-2-{2[2-(1-methoxycarbonylethoxy)phenyl]vinyl}-1-methylindole | HCID 69953350 | 90% |
反応手順
To a solution of 1.50 g (6.02 mmol) of 2-[2-(2-hydroxyphenyl)vinyl]-1-methylindole, 1.89 g (7.21 mmol) of triphenylphosphine and 0.69 ml (7.22 mmol) of R-(+)-methyl lactate in 15 ml of THF was added 1.14 ml (7.24 mmol) of diethylazodicarboxylate under an ice-cooled condition, followed by stirring at room temperature for 2 hours. Brine was added to the reaction mixture, followed by extraction with methylene chloride. The extract was dried over Na2SO4, and evaporated. CHCl3 -n-hexane was added to the residue and, after filtration, the organic layer was purified by silica gel column chromatography (CHCl3 /n-hexane/AcOEt=10/10/1) to give 1.82 g (90%) of (S)-2-{2[2-(1-methoxycarbonylethoxy)phenyl]vinyl}-1-methylindole.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05728709 |
| 出典データセット | uspto-grants-1998_03 |
| ORD ID | ord-45b51dfa48a4401f8cc762580c573748 |
| 出典メモ | uspto-grants-1998_03 |