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Sodium Carbonate → (2R,5S)-Dimethyl 1-(2-(1,3-dioxoisoindolin-2-yl)ethyl)piperidine-2,5-dicarboxylate

HRID 1683317
ノート
印刷プレビュー

反応式

HRID 1683317 の反応式
C(=O)([O-])[O-].[Na+].[Na+].O([CH2:15][CH2:16][N:17]1[C:21](=[O:22])[C:20]2=[CH:23][CH:24]=[CH:25][CH:26]=[C:19]2[C:18]1=[O:27])S(C(F)(F)F)(=O)=O.Cl.[CH3:29][O:30][C:31]([C@H:33]1[CH2:38][CH2:37][C@H:36]([C:39]([O:41][CH3:42])=[O:40])[CH2:35][NH:34]1)=[O:32]>O.C(Cl)Cl>[C:21]1(=[O:22])[N:17]([CH2:16][CH2:15][N:34]2[CH2:35][C@@H:36]([C:39]([O:41][CH3:42])=[O:40])[CH2:37][CH2:38][C@@H:33]2[C:31]([O:30][CH3:29])=[O:32])[C:18](=[O:27])[C:19]2=[CH:26][CH:25]=[CH:24][CH:23]=[C:20]12
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 10340Sodium CarbonateHCID 118094652-(1,3-Dioxoisoindolin-2-yl)ethyl trifluoromethanesulfonateHCID 67703709trans-2,5-Piperidine dicarboxylate dimethyl ester hydrochloride

生成物 1

HCID 21782948(2R,5S)-Dimethyl 1-(2-(1,3-dioxoisoindolin-2-yl)ethyl)piperidine-2,5-dicarboxylate収率 99.1%

試薬・触媒・溶媒 2

HCID 962Water
溶媒
HCID 6344Dichloromethane溶媒2 回

実験手順

To a well-stirred bi-phasic mixture consisting of sodium carbonate (500 g, 4.72 mol) in water (3 liters) and trans-2,5-piperidine dicarboxylate dimethyl ester hydrochloride (280 g, 1.18 mol in methylene chloride (4.5 liters), a solution of 2-phthalimido-ethyl triflate (417 g, 1.29 mol) in methylene chloride (3 liters) was added in a steady stream over a 3 hour period. The organic layer was separated, and the aqueous layer was extracted with fresh methylene chloride (3 liters). The combined organic extracts were washed with water (3 liters), then with brine (3 liters), dried with anhydrous magnesium sulfate and finally, concentrated in vacuo to a solid. The entire residue was triturated in resulting ether (3 liters), with vigorous stirring, for 15 minutes. After cooling to ambient temperature, the solution was poured into hexanes (3 liters), and the resulting mixture was stirred for 18 hours. The resulting colorless solid was collected by filtration, and the filter cake was washed with hexanes (1 liter). In vacuo drying afforded 437.3 g (99.1% yield) of the title compound as a colorless solid. TLC Rf (ethyl acetate/methylene chloride=1:1 in volume; iodoplatinate spray): 0.5.

後処理

  1. customThe organic layer was separated
  2. extractionthe aqueous layer was extracted with fresh methylene chloride (3 liters)
  3. washThe combined organic extracts were washed with water (3 liters)
  4. dry with materialwith brine (3 liters), dried with anhydrous magnesium sulfate
  5. concentrationfinally, concentrated in vacuo to a solid
  6. customThe entire residue was triturated
  7. customin resulting ether (3 liters)
  8. filtrationThe resulting colorless solid was collected by filtration
  9. washthe filter cake was washed with hexanes (1 liter)
  10. customIn vacuo drying

出典と根拠

ORDレコード
ord-e3afcb94d2284800ab06f20d15406222
出典データセット
uspto-grants-1997_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05637713

反応ノート

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