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Morpholine → Ethyl 4-morpholinepropionate

HRID 1955647
ノート
印刷プレビュー

反応式

HRID 1955647 の反応式
[CH2:1]([O:3][C:4](=[O:8])[CH2:5][CH2:6]Br)[CH3:2].[NH:9]1[CH2:14][CH2:13][O:12][CH2:11][CH2:10]1.C([O-])([O-])=O.[Na+].[Na+]>CCO>[CH2:1]([O:3][C:4](=[O:8])[CH2:5][CH2:6][N:9]1[CH2:14][CH2:13][O:12][CH2:11][CH2:10]1)[CH3:2]
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 8083MorpholineHCID 10340Sodium CarbonateHCID 68320Ethyl 3-bromopropionate

生成物 1

HCID 88374Ethyl 4-morpholinepropionate収率 101.5%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

Ethyl-3-bromoproprionate (3.20 ml; 25 mmol) was added to a mixture of morpholine (2.20 ml; 25 mmol) and Na2CO3 (2.78 g; 26 mmol) in 4.5 ml of EtOH at RT. The mixture was stirred for 30 min at RT and 4 h at reflux. After cooling to RT and filtering, the filtrate was concentrated and the residue was dissolved in H2O. The pH was adjusted to ~1.5 with saturated KHSO4 and the acidic mixture was washed with Et2O. Solid K2CO3 was added to the aqueous layer until a pH of ~9 was reached. The basic mixture was extracted with CH2Cl2, dried (MgSO4) and concentrated to afford 4.75 g (100+%; contained trace solvent) of ethyl-3-morpholinoproprionate as a colorless liquid. A solution of this ester (935 mg; 5 mmol) in 20 ml of Et2O was added to a suspension of LiAlH4 (400 mg; 10 mmol) in 80 ml of Et2O at 0° C. After stirring for 30 min at 0° C., the reaction was quenched by the careful addition of 0.42 ml of H2O followed by 0.42 ml of 15% NaOH and 1.26 ml of H2O. MgSO4 was added and the suspension was filtered and concentrated to afford 531 mg (73%) of Compound 201a as a colorless liquid. ##STR383##

後処理

  1. temperatureat reflux
  2. temperatureAfter cooling to RT
  3. filtrationfiltering
  4. concentrationthe filtrate was concentrated
  5. dissolutionthe residue was dissolved in H2O
  6. washthe acidic mixture was washed with Et2O
  7. additionSolid K2CO3 was added to the aqueous layer until a pH of ~9
  8. extractionThe basic mixture was extracted with CH2Cl2
  9. dry with materialdried (MgSO4)
  10. concentrationconcentrated

出典と根拠

ORDレコード
ord-295cb27742a64161a585420ce4aa76a0
出典データセット
uspto-grants-1998_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05776933

反応ノート

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