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Methyl iodide → tert-butyl [(2R)-2-methoxypropyl]carbamate

HRID 1948388
ノート
印刷プレビュー

反応式

HRID 1948388 の反応式
[OH:1][C@H:2]([CH3:12])[CH2:3][NH:4][C:5](=[O:11])[O:6][C:7]([CH3:10])([CH3:9])[CH3:8].[H-].[Na+].[CH3:15]I>C1COCC1>[CH3:15][O:1][C@H:2]([CH3:12])[CH2:3][NH:4][C:5](=[O:11])[O:6][C:7]([CH3:8])([CH3:10])[CH3:9]
参加物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 24758Sodium hydrideHCID 12094522N-Boc-(R)-1-amino-2-propanol

生成物 1

HCID 86641515tert-butyl [(2R)-2-methoxypropyl]carbamate

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

To a solution of tert-butyl [(2R)-2-hydroxypropyl]carbamate (0.4 g, 2.28 mmol) in THF (5 mL), sodium hydride (0.06 g, 2.51 mmol) was added at 0° C. The resulting solution was stirred for 30 minutes at that temperature and then methyl iodide (0.14 mL, 2.28 mmol) was added. The reaction was warmed to room temperature slowly and allowed to stir for an additional two hours. The reaction was quenched by adding water and extracted with ethyl acetate. The extract was washed with sodium bicarbonate solution, water and brine. It was dried over magnesium sulfate and concentrated. The desired product was obtained as clear oil (0.31 g) and it did not need any further purification.

後処理

  1. stirringto stir for an additional two hours
  2. customThe reaction was quenched
  3. additionby adding water
  4. extractionextracted with ethyl acetate
  5. washThe extract was washed with sodium bicarbonate solution, water and brine
  6. dry with materialIt was dried over magnesium sulfate
  7. concentrationconcentrated

出典と根拠

ORDレコード
ord-970a343624754a1084a645a79af878a1
出典データセット
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08399489B2

反応ノート

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