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3-Cyclohexene-1,2-dicarboxylic acid → cis-1,2-Dihydroxymethylcyclohex-4-ene

HRID 1982490
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HRID 1982490 반응식
[C:1]([CH:4]1[CH:9]([C:10](O)=[O:11])[CH2:8][CH2:7][CH:6]=[CH:5]1)(O)=[O:2].[H-].[Al+3].[Li+].[H-].[H-].[H-].C1COCC1.O>C1COCC1.C1C=CC=CC=1>[OH:2][CH2:1][C@H:4]1[C@@H:9]([CH2:10][OH:11])[CH2:8][CH:7]=[CH:6][CH2:5]1
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참가 물질

6

반응물 3

HCID 127266073-Cyclohexene-1,2-dicarboxylic acidHCID 21226445Aluminium lithium hydrideHCID 21881883Oxolane--water (1/1)

생성물 1

HCID 11275057cis-1,2-Dihydroxymethylcyclohex-4-ene수율 102%

시약·촉매·용매 2

HCID 241Benzene용매HCID 8028Tetrahydrofuran
용매
2회

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온도
0 °C

실험 절차

A solution of the anhydride of 3,4-dicarboxycyclohex-1-ene (25.8 g) in THF (150 ml) is added with cooling to a stirred suspension of LiA1H4 (9 g) in THF (200 ml) under N2 at a rate such as to maintain the temperature at 0° C. After stirring for 18 hours at room temperature the mixture is gently refluxed for one hour and cooled in ice. The excess lithium aluminium hydride is decomposed by the careful addition of 1:1 THF-H2O mixture (100 ml). After dilution with chloroform (150 ml) the resulting mixture is filtered and the solid is washed with chloroform (3×25 ml). Concentration of the filtrate under reduced pressure yields an oily residue which is dissolved in benzene, dried over (MgSO4) and reconcentrated in vacuo to give the title compound as an oil (22 g, ca. 90%), λmax (film) 3350 cm-1.

후처리

  1. temperatureis gently refluxed for one hour
  2. temperaturecooled in ice
  3. filtrationAfter dilution with chloroform (150 ml) the resulting mixture is filtered
  4. washthe solid is washed with chloroform (3×25 ml)
  5. customConcentration of the filtrate under reduced pressure yields an oily residue which
  6. dry with materialdried over (MgSO4)

출처 및 근거

ORD 기록
ord-8928b9d61c8e477080e41611e5814b12
출처 데이터셋
uspto-grants-1986_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04596823

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