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HRID 658233作成日:2026年10月24日
Tributylphosphine → 4-{4-[2-(2,6-Dichloro-4-methylphenoxy)ethoxy]phenyl}piperidine-1,3-dicarboxylic acid 1-tert-butyl ester 3-methyl ester
https://huagongshe.com/ja/reaction/658233
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Tributylphosphine | HCID 13831 | — |
| 反応物 | 2,6-Dichloro-4-methylphenol | HCID 17077 | — |
| 反応物 | 4-[4-(2-Hydroxyethoxy)phenyl]piperidine-1,3-dicarboxylic acid 1-tert-butyl ester 3-methyl ester | HCID 68426240 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 4-{4-[2-(2,6-Dichloro-4-methylphenoxy)ethoxy]phenyl}piperidine-1,3-dicarboxylic acid 1-tert-butyl ester 3-methyl ester | HCID 67148722 | 90.4% |
反応手順
A mixture of compound 4-[4-(2-Hydroxyethoxy)phenyl]piperidine-1,3-dicarboxylic acid 1-tert-butyl ester 3-methyl ester (5.50 g, 15 mmol), 2,6-dichloro-p-cresol (3.08 g, 18 mmol), azodicarboxylic dipiperidine (7.31 g, 29 mmol) and PBu3 (14 mL, 58 mmol) in toluene (150 mL) was heated to 50° C. for 16 h. The mixture was allowed to cool to rt, filtered, and the precipitate was washed with toluene. The filtrate was diluted with EtOAc, and washed with water (2×) and brine. The org. layer was dried over MgSO4, filtered, and the solvents were removed under reduced pressure. Purification of the crude by FC (EtOAc/heptane 0:1→1:9→2:8) yielded the compound as a colorless oil (7.3 g, 90%). LC-MS: tR=1.18 min, ES+=538.34.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08076359B2 |
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| 出典データセット | uspto-grants-2011_12 |
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| ORD ID | ord-0601ea16034042da90eac4477089c26d |
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| 出典メモ | uspto-grants-2011_12 |
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