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Ethylacetate heptane → 3-Fluoro-2-(3-hydroxypropyl)-6-methoxyphenol

HRID 1157929
ノート
印刷プレビュー

反応式

HRID 1157929 の反応式
[F:1][C:2]1[C:7]([CH:8]=O)=[C:6]([OH:10])[C:5]([O:11][CH3:12])=[CH:4][CH:3]=1.CCCCCCC.[C:20](OCC)(=[O:22])[CH3:21]>ClCCl>[F:1][C:2]1[C:7]([CH2:8][CH2:21][CH2:20][OH:22])=[C:6]([OH:10])[C:5]([O:11][CH3:12])=[CH:4][CH:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 21899848Ethylacetate heptaneHCID 224828186-Fluoro-2-hydroxy-3-methoxybenzaldehyde

生成物 1

HCID 595119113-Fluoro-2-(3-hydroxypropyl)-6-methoxyphenol

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

To a 50 ml solution of 4.46 g of 6-fluoro-2-hydroxy-3-methoxybenzaldehyde in dichloromethane there was added 10 g of (triphenylphosphoranilidene)acetic acid ethyl ester while cooling on ice. After stirring at room temperature for 30 minutes, the reaction mixture was poured into a silica gel column and elution was performed with heptane-ethyl acetate=3:1. The eluate was concentrated under reduced pressure. The residue was dissolved in 100 ml of ethyl acetate, and 1 g of 10% palladium-carbon was added prior to stirring for 7 hours at room temperature under a hydrogen atmosphere. The reaction mixture was filtered through Celite, and the filtrate was concentrated under reduced pressure. The residue was dissolved in 100 ml of THF, 2 g of lithium borohydride was added while cooling on ice and the mixture was stirred overnight at room temperature. After then adding 1N hydrochloric acid to the reaction mixture while cooling on ice, extraction was performed with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate. The desiccant was filtered out and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate-heptane system) to obtain the target compound (4.78 g) as a solid.

後処理

  1. temperaturewhile cooling on ice
  2. additionthe reaction mixture was poured into a silica gel column and elution
  3. concentrationThe eluate was concentrated under reduced pressure
  4. dissolutionThe residue was dissolved in 100 ml of ethyl acetate
  5. addition1 g of 10% palladium-carbon was added
  6. stirringto stirring for 7 hours at room temperature under a hydrogen atmosphere
  7. filtrationThe reaction mixture was filtered through Celite
  8. concentrationthe filtrate was concentrated under reduced pressure
  9. dissolutionThe residue was dissolved in 100 ml of THF
  10. addition2 g of lithium borohydride was added
  11. temperaturewhile cooling on ice
  12. stirringthe mixture was stirred overnight at room temperature
  13. additionAfter then adding 1N hydrochloric acid to the reaction mixture
  14. temperaturewhile cooling on ice, extraction
  15. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  16. filtrationThe desiccant was filtered out
  17. concentrationthe filtrate was concentrated under reduced pressure
  18. customThe residue was purified by silica gel column chromatography (ethyl acetate-heptane system)

出典と根拠

ORDレコード
ord-5fd76229d9d74545a76578ca4b4b6779
出典データセット
uspto-grants-2010_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07807690B2

反応ノート

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