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Sodium Hydroxide → Trans 4-(2-Chloro-4-fluoro-phenoxy)-3-hydroxy-piperidine-1-carboxylic acid tert-butyl ester

HRID 1714403
ノート
印刷プレビュー

反応式

HRID 1714403 の反応式
[C:1]([O:5][C:6]([N:8]1[CH2:14][CH2:13][C@@H:12]2[C@@H:10]([O:11]2)[CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[Cl:15][C:16]1[CH:21]=[C:20]([F:22])[CH:19]=[CH:18][C:17]=1[OH:23].[OH-].[Na+].[Cl-].[NH4+]>O1CCOCC1.CCCCCCC.C(OCC)(=O)C>[C:1]([O:5][C:6]([N:8]1[CH2:14][CH2:13][C@@H:12]([O:23][C:17]2[CH:18]=[CH:19][C:20]([F:22])=[CH:21][C:16]=2[Cl:15])[C@H:10]([OH:11])[CH2:9]1)=[O:7])([CH3:4])([CH3:2])[CH3:3]
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 14798Sodium HydroxideHCID 25517Ammonium ChlorideHCID 748142-Chloro-4-fluorophenolHCID 55273474tert-butyl (1S,6R)-7-oxa-3-azabicyclo[4.1.0]heptane-3-carboxylate

生成物 1

HCID 68506255Trans 4-(2-Chloro-4-fluoro-phenoxy)-3-hydroxy-piperidine-1-carboxylic acid tert-butyl ester

試薬・触媒・溶媒 2

HCID 31275
1,4-Dioxane
溶媒
HCID 21899848Ethylacetate heptane溶媒2 回

実験手順

Rac-cis-7-Oxa-3-aza-bicyclo[4.1.0]heptane-3-carboxylic acid tert-butyl ester (1 g, 5 mmol) was solvated in dioxane (5 mL), 2-Chloro-4-Fluorophenol was added (1.471 g, 10 mmol) and sodium hydroxide (0.401 g, 10 mmol). After 20 hours refluxing, the mixture was cooled, ammonium chloride was added and the mixture extracted three times with ethyl acetate. The combined organic phases were dried with magnesium sulfate and concentrated under vacuum. After a flash chromatography with heptane/ethyl acetate 1:1 to 1:2 heptane/ethyl acetate a solid the title compound was obtained as solid (0.778 g, 45% yield). MS (m/e): 404.5 (M+AcO−).

後処理

  1. temperatureAfter 20 hours refluxing
  2. temperaturethe mixture was cooled
  3. extractionthe mixture extracted three times with ethyl acetate
  4. dry with materialThe combined organic phases were dried with magnesium sulfate
  5. concentrationconcentrated under vacuum

出典と根拠

ORDレコード
ord-0f043f77be3f4268a079654f59e3fdfa
出典データセット
uspto-grants-2010_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07795437B2

反応ノート

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