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Methyl iodide → 2-methyl-3-(N-Boc-piperidine-4-yl)-propionic acid methyl ester

HRID 1691856
ノート
印刷プレビュー

反応式

HRID 1691856 の反応式
[CH3:1][O:2][C:3](=[O:19])[CH2:4][CH2:5][CH:6]1[CH2:11][CH2:10][N:9]([C:12]([O:14][C:15]([CH3:18])([CH3:17])[CH3:16])=[O:13])[CH2:8][CH2:7]1.[CH3:20][Si]([N-][Si](C)(C)C)(C)C.[Na+].CI>O1CCCC1>[CH3:1][O:2][C:3](=[O:19])[CH:4]([CH3:20])[CH2:5][CH:6]1[CH2:11][CH2:10][N:9]([C:12]([O:14][C:15]([CH3:16])([CH3:18])[CH3:17])=[O:13])[CH2:8][CH2:7]1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 6328Methyl iodideHCID 1502093Methyl N-Boc-4-piperidinepropionateHCID 2724254Sodium bis(trimethylsilyl)amide

生成物 1

HCID 592610702-methyl-3-(N-Boc-piperidine-4-yl)-propionic acid methyl ester

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
-78 °C

実験手順

3-(N-Boc-piperidine-4-yl)-propionic acid methyl ester (2.0 g, 7.38 mmol) from above was dissolved in tetrahydrofuran (50 mL). The solution was cooled to −78° C. and sodium bis(trimethylsilyl)amide (1.0 M, 9.0 mL) was added. The mixture was stirred at −78° C. for 1 hr and methyl iodide (1.2 mL, 19.5 mmol) was added. The mixture was warmed to room temperature and stirred for 2 hrs. The mixture was extracted with ether and washed with dilute hydrochloric acid. The organic layer was dried, filtered and concentrated. The residue was purified using flash chromatography (eluting with ethyl acetate and hexanes) to give 2-methyl-3-(N-Boc-piperidine-4-yl)-propionic acid methyl ester as an oil (789 mg).

後処理

  1. temperatureThe mixture was warmed to room temperature
  2. stirringstirred for 2 hrs
  3. extractionThe mixture was extracted with ether
  4. washwashed with dilute hydrochloric acid
  5. customThe organic layer was dried
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customThe residue was purified
  9. washflash chromatography (eluting with ethyl acetate and hexanes)

出典と根拠

ORDレコード
ord-9a4deedac40b4f63a9c1bcdeb98616a8
出典データセット
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08153644B2

反応ノート

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