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Aluminium lithium hydride → (5-phenyl-3,6-dihydro-2H-pyran-4-yl)methanol

HRID 1484795
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HRID 1484795 반응식
[C:1]1([C:7]2[CH2:12][O:11][CH2:10][CH2:9][C:8]=2[C:13](OCC)=[O:14])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[H-].[H-].[H-].[H-].[Li+].[Al+3]>C1COCC1>[C:1]1([C:7]2[CH2:12][O:11][CH2:10][CH2:9][C:8]=2[CH2:13][OH:14])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1
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참가 물질

4

반응물 2

HCID 21226445Aluminium lithium hydrideHCID 67311476ethyl 5-phenyl-3,6-dihydro-2H-pyran-4-carboxylate

생성물 1

HCID 90417308(5-phenyl-3,6-dihydro-2H-pyran-4-yl)methanol수율 83.7%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
-20 °C

실험 절차

To a solution of ethyl 5-phenyl-3,6-dihydro-2H-pyran-4-carboxylate (1.05 g, 4.52 mmol) in THF (20 mL) was added LiAlH4 (1M in THF, 5.42 mL, 5.42 mmol) at −20° C., the reaction was stirred at −20° C. for 30 min, and was quenched with Sat. NH4Cl, the aqueous layer was extracted with EtOAc, the combined organics were washed with brine, dried and concentrated to give crude oil, which was purified by column (Hexanes/EtOAc=100:0 to 35:65) to give (5-phenyl-3,6-dihydro-2H-pyran-4-yl)methanol (720 mg).

후처리

  1. customwas quenched with Sat. NH4Cl
  2. extractionthe aqueous layer was extracted with EtOAc
  3. washthe combined organics were washed with brine
  4. customdried
  5. concentrationconcentrated
  6. customto give crude oil, which
  7. customwas purified by column (Hexanes/EtOAc=100:0 to 35:65)

출처 및 근거

ORD 기록
ord-fe017942113f4bc1a8e55fde8b49eecc
출처 데이터셋
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09422279B2

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