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Water → (RS)-1,1-Dimethylethyl 4-(1,2-Dihydroxyethyl)-4-(phenylmethoxymethyl)-1-piperidinecarboxylate

HRID 2213031
ノート
印刷プレビュー

反応式

HRID 2213031 の反応式
[CH:1]([C:3]1([CH2:16][O:17][CH2:18][C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[CH2:8][CH2:7][N:6]([C:9]([O:11][C:12]([CH3:15])([CH3:14])[CH3:13])=[O:10])[CH2:5][CH2:4]1)=[CH2:2].C[N+]1([O-])CC[O:29]CC1.S([O-])(O)(=O)=O.[Na+].[OH2:39]>O1CCCC1.[Os](=O)(=O)(=O)=O>[OH:39][CH:1]([C:3]1([CH2:16][O:17][CH2:18][C:19]2[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=2)[CH2:8][CH2:7][N:6]([C:9]([O:11][C:12]([CH3:15])([CH3:13])[CH3:14])=[O:10])[CH2:5][CH2:4]1)[CH2:2][OH:29]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 962WaterHCID 82029Methyl morpholine oxideHCID 516919Sodium BisulfateHCID 219553091,1-Dimethylethyl 4-Ethenyl-4-(phenylmethoxymethyl)-1-piperidinecarboxylate

生成物 1

HCID 21955196(RS)-1,1-Dimethylethyl 4-(1,2-Dihydroxyethyl)-4-(phenylmethoxymethyl)-1-piperidinecarboxylate収率 96%

試薬・触媒・溶媒 2

HCID 30318
Osmium Tetroxide
触媒
HCID 8028Tetrahydrofuran溶媒

実験手順

Osmium tetroxide (2.5 wt % solution in tert-butanol, 240 mL) was added to a mixture of 1,1-dimethylethyl 4-ethenyl-4-(phenylmethoxymethyl)-1-piperidinecarboxylate (Description 96, 1.01 g, 3 mmol) and N-methylmorpholine-N-oxide (460 mg, 4 mmol) in water (4 mL) and tetrahydrofuran (12 mL). The mixture was stirred at room temperature for 24 hours then saturated aqueous sodium hydrogen sulphate (5 mL) was added. The mixture was extracted with ethyl acetate (2×15 mL), the combined organic fractions were dried (MgSO4) and the solvent was evaporated under reduced pressure to give the title compound (1.05 g, 96%). m/z (ES+) 366 (M+1).

後処理

  1. extractionThe mixture was extracted with ethyl acetate (2×15 mL)
  2. dry with materialthe combined organic fractions were dried (MgSO4)
  3. customthe solvent was evaporated under reduced pressure

出典と根拠

ORDレコード
ord-3be7c58a40dd4f948d7aa7f17f8a93bc
出典データセット
uspto-grants-2006_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07105507B2

反応ノート

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