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Hydrochloric Acid → 2,2-Dibutyl-5-hydroxy-1,2,3,4-tetrahydro-1-naphthol

HRID 727811
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HRID 727811 반응식
[CH2:1]([C:5]1([CH2:17][CH2:18][CH2:19][CH3:20])[CH2:14][CH2:13][C:12]2[C:7](=[CH:8][CH:9]=[CH:10][C:11]=2[OH:15])[C:6]1=[O:16])[CH2:2][CH2:3][CH3:4].[H-].[Al+3].[Li+].[H-].[H-].[H-].Cl>C(OCC)C>[CH2:1]([C:5]1([CH2:17][CH2:18][CH2:19][CH3:20])[CH2:14][CH2:13][C:12]2[C:7](=[CH:8][CH:9]=[CH:10][C:11]=2[OH:15])[CH:6]1[OH:16])[CH2:2][CH2:3][CH3:4]
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참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 10659962HCID 10659962, 화합물HCID 21226445Aluminium lithium hydride

생성물 1

HCID 105166192,2-Dibutyl-5-hydroxy-1,2,3,4-tetrahydro-1-naphthol수율 93.7%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

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온도
0 °C

실험 절차

To a solution of 2,2-dibutyl-3,4-dihydro-5-hydroxy-1(2H)-naphthalenone (9.59 g) in dry diethyl ether (100 ml) was added lithium aluminium hydride (1.33 g) slowly at 0° C. under a nitrogen atmosphere. The suspension was stirred for 3 hours at 0° C. and then poured into ice. The mixture was acidified with aqueous 1N hydrochloric acid and the separated oil was extracted with diethyl ether. The extract was washed with brine and aqueous sodium bicarbonate solution. The solvent was dried and concentrated in vacuo. The residue was purified by columnchromatography on silica gel (elution by CH2Cl2 and then 2% CH3OH in CH2Cl2) to yield 2,2-dibutyl-5-hydroxy-1,2,3,4-tetrahydro-1-naphthol (9.05 g) as crystals.

후처리

  1. additionpoured into ice
  2. extractionthe separated oil was extracted with diethyl ether
  3. washThe extract was washed with brine and aqueous sodium bicarbonate solution
  4. customThe solvent was dried
  5. concentrationconcentrated in vacuo
  6. customThe residue was purified by columnchromatography on silica gel (
  7. washelution by CH2Cl2

출처 및 근거

ORD 기록
ord-db49a2c05d1a4bd9a676576a7b62344e
출처 데이터셋
uspto-grants-1991_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05045548

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