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Triphenylphosphine → 2-[9-(1H-pyrazol-1-yl)-6-oxaspiro[4.5]decan-9-yl]acetaldehyde

HRID 626488
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HRID 626488 반응식
[CH2:1]([C:4]1([N:14]2[CH:18]=[CH:17][CH:16]=[N:15]2)[CH2:13][C:8]2([CH2:12][CH2:11][CH2:10][CH2:9]2)[O:7][CH2:6][CH2:5]1)[CH:2]=C.[O:19]=[O+][O-].C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>C(Cl)Cl>[N:14]1([C:4]2([CH2:1][CH:2]=[O:19])[CH2:13][C:8]3([CH2:12][CH2:11][CH2:10][CH2:9]3)[O:7][CH2:6][CH2:5]2)[CH:18]=[CH:17][CH:16]=[N:15]1
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참가 물질

5

반응물 3

HCID 11776TriphenylphosphineHCID 24823OzoneHCID 683141651-[9-(prop-2-en-1-yl)-6-oxaspiro[4.5]decan-9-yl]-1H-pyrazole

생성물 1

HCID 866714282-[9-(1H-pyrazol-1-yl)-6-oxaspiro[4.5]decan-9-yl]acetaldehyde수율 23%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a solution of 1-[9-(prop-2-en-1-yl)-6-oxaspiro[4.5]decan-9-yl]-1H-pyrazole (80 mg, 0.32 mmol) in DCM (5 mL) at −78° C. was bubbled with O3 until the solution turned blue. The resulting solution was bubbled with N2 for 5 min. To it was added PPh3 (168 mg, 0.64 mmol). And the solution was stirred for 4 h at rt. After removal of the solvent, the residue was purified by flash column chromatography to give 2-[9-(1H-pyrazol-1-yl)-6-oxaspiro[4.5]decan-9-yl]acetaldehyde (15 mg, 23% yield). LCMS m/z 249 (M+1) observed.

후처리

  1. customThe resulting solution was bubbled with N2 for 5 min
  2. customAfter removal of the solvent
  3. customthe residue was purified by flash column chromatography

출처 및 근거

ORD 기록
ord-9f88dd2b9453439ba6dc684343a24b28
출처 데이터셋
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09309234B2

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