7-(Pyridin-4-ylmethoxy)-1,2,3,4-tetrahydronaphthalen-1-one → 7-(Pyridin-4-ylmethoxy)-1,2,3,4-tetrahydronaphthalen-1-ol

HRID 2394326

반응식

HRID 2394326 반응식
[N:1]1[CH:6]=[CH:5][C:4]([CH2:7][O:8][C:9]2[CH:18]=[C:17]3[C:12]([CH2:13][CH2:14][CH2:15][C:16]3=[O:19])=[CH:11][CH:10]=2)=[CH:3][CH:2]=1.[H-].C([Al+]CC(C)C)C(C)C>O1CCCC1.C1(C)C=CC=CC=1>[N:1]1[CH:6]=[CH:5][C:4]([CH2:7][O:8][C:9]2[CH:18]=[C:17]3[C:12]([CH2:13][CH2:14][CH2:15][CH:16]3[OH:19])=[CH:11][CH:10]=2)=[CH:3][CH:2]=1

참가 물질

5

반응물 2

HCID 189732117-(Pyridin-4-ylmethoxy)-1,2,3,4-tetrahydronaphthalen-1-oneHCID 21225700Diisobutylaluminumhydride

생성물 1

HCID 189732197-(Pyridin-4-ylmethoxy)-1,2,3,4-tetrahydronaphthalen-1-ol수율 78.2%

시약·촉매·용매 2

HCID 1140Toluene용매HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of Compound 1 (16.41 g, 64.9 mmol) in tetrahydrofuran (75 mL) at 0° C. was added dropwise a 1M solution of diisobutylaluminum hydride in toluene (97.3 mL). After 1 hr, the reaction was quenched with aqueous potassium sodium tartrate and diluted with ethyl acetate followed by warming to room temperature. After stirring for an additional hour, the layers were separated and the aqueous phase was re-extracted with ethyl acetate (2×). The extracts were combined, washed with brine, dried over anh. magnesium sulfate, filtered and concentrated in vacuo. Chromatography of the residue on silica gel (elution with ethyl acetate) provided 12.96 g of Compound 2 as an oil which crystallized upon standing.

후처리

  1. customthe reaction was quenched with aqueous potassium sodium tartrate
  2. additiondiluted with ethyl acetate
  3. customthe layers were separated
  4. extractionthe aqueous phase was re-extracted with ethyl acetate (2×)
  5. washwashed with brine
  6. dry with materialdried over anh. magnesium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-18649a9d73224d33be90767d3564d14d
출처 데이터셋
uspto-grants-1998_09
특허 번호
US05811434

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