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Bromoacetonitrile → (R)-tert-butyl 2-((S)-(3-chlorophenyl)(cyanomethoxy)methyl)morpholine-4-carboxylate

HRID 253589
ノート
印刷プレビュー

反応式

HRID 253589 の反応式
[Cl:1][C:2]1[CH:3]=[C:4]([C@H:8]([OH:22])[C@@H:9]2[O:14][CH2:13][CH2:12][N:11]([C:15]([O:17][C:18]([CH3:21])([CH3:20])[CH3:19])=[O:16])[CH2:10]2)[CH:5]=[CH:6][CH:7]=1.[H-].[Na+].Br[CH2:26][C:27]#[N:28]>CC#N>[Cl:1][C:2]1[CH:3]=[C:4]([C@H:8]([O:22][CH2:26][C:27]#[N:28])[C@@H:9]2[O:14][CH2:13][CH2:12][N:11]([C:15]([O:17][C:18]([CH3:19])([CH3:21])[CH3:20])=[O:16])[CH2:10]2)[CH:5]=[CH:6][CH:7]=1
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 11534BromoacetonitrileHCID 24758Sodium hydrideHCID 57786497(R)-tert-butyl 2-((S)-(3-chlorophenyl)(hydroxy)methyl)morpholine-4-carboxylate

生成物 1

HCID 66862450(R)-tert-butyl 2-((S)-(3-chlorophenyl)(cyanomethoxy)methyl)morpholine-4-carboxylate

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒

実験手順

To a solution of (R)-tert-butyl 2-((S)-(3-chlorophenyl)(hydroxy)methyl)morpholine-4-carboxylate (1.3 g, 3.98 mmol) in MeCN (20 mL), NaH (230 mg, 9.55 mmol) was added at 0° C. The mixture was stirred for 1 h at rt. The mixture was cooled to −40° C., and bromoacetonitrile (1.14 g, 9.55 mmol) was added in portions. The mixture was stirred for 0.5 h at −20° C. The solution was evaporated and H2O (50 mL) was added. 1N aq HCl was added and the mixture was extracted with CH2Cl2. The organic layer was washed with aq NaHCO3 and brine, dried over Na2SO4 and concentrated. The crude product was used directly in the next step.

後処理

  1. temperatureThe mixture was cooled to −40° C.
  2. stirringThe mixture was stirred for 0.5 h at −20° C
  3. customThe solution was evaporated
  4. additionH2O (50 mL) was added
  5. addition1N aq HCl was added
  6. extractionthe mixture was extracted with CH2Cl2
  7. washThe organic layer was washed with aq NaHCO3 and brine
  8. dry with materialdried over Na2SO4
  9. concentrationconcentrated

出典と根拠

ORDレコード
ord-edc1c239f44f40e5887eef213af0b5b1
出典データセット
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07872028B2

反応ノート

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