Sodium Hydroxide → HCID 57827596, compound

HRID 1693147Notes

Reaction equation

HRID 1693147 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[CH2:12][CH2:11][CH2:10][C:9]=1[C:13](OCC)=[O:14].[H-].[Al+3].[Li+].[H-].[H-].[H-].[OH-].[Na+].S([O-])([O-])(=O)=O.[Mg+2]>C1COCC1.O>[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[CH2:12][CH2:11][CH2:10][C:9]=1[CH2:13][OH:14]

Participants

7

Procedure

A solution of ethyl 2-(2-fluorophenyl)cyclopent-1-enecarboxylate obtained in Preparation Example 3-(2) (7.60 g) in THF (100 mL) was added dropwise to a suspension of lithium aluminum hydride (1.34 g) in THF (300 mL) in an ice bath. The reaction solution was stirred at the same temperature for one hour. Then, water (1.35 mL), a 5 N sodium hydroxide solution (1.35 mL) and water (4.05 mL) were sequentially added dropwise in an ice bath. Anhydrous magnesium sulfate was added to the generated reaction mixture, followed by extraction with ethyl acetate. The reaction mixture was filtered through celite and the filtrate was concentrated under reduced pressure to obtain a residue. The residue was purified by silica gel column chromatography to obtain the title compound (6.50 g).

Workup

  1. extractionfollowed by extraction with ethyl acetate
  2. filtrationThe reaction mixture was filtered through celite
  3. concentrationthe filtrate was concentrated under reduced pressure
  4. customto obtain a residue
  5. customThe residue was purified by silica gel column chromatography

Sources & evidence

ORD record
ord-82d6cc90ee7f4b6b821a041c743841c0
Source dataset
uspto-grants-2012_04
Patent number
US08158620B2

Reaction notes

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