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Methanol → 1-(4-Methoxybenzyl)piperidine-4-carboxaldehyde

HRID 424617
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HRID 424617 반응식
[H-].C([Al+]CC(C)C)C(C)C.[CH3:11][O:12][C:13]1[CH:29]=[CH:28][C:16]([CH2:17][N:18]2[CH2:23][CH2:22][CH:21]([C:24](OC)=[O:25])[CH2:20][CH2:19]2)=[CH:15][CH:14]=1.CO.[Cl-].[Na+]>C1(C)C=CC=CC=1>[CH3:11][O:12][C:13]1[CH:14]=[CH:15][C:16]([CH2:17][N:18]2[CH2:23][CH2:22][CH:21]([CH:24]=[O:25])[CH2:20][CH2:19]2)=[CH:28][CH:29]=1
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참가 물질

6

반응물 4

HCID 887MethanolHCID 5234Sodium ChlorideHCID 21225700DiisobutylaluminumhydrideHCID 60704011HCID 60704011, 화합물

생성물 1

HCID 178939301-(4-Methoxybenzyl)piperidine-4-carboxaldehyde

시약·촉매·용매 1

HCID 1140Toluene용매2회

실험 절차

A 1.5 M solution of diisobutylaluminium hydride in toluene (3.12 ml, 4.68 mmol) was added dropwise to a solution of methyl 1-(4-methoxybenzyl)piperidine-4-carboxylate (1.23 g, 4.68 mmol) in toluene (30 ml) under argon at −78° C. in the course of 30 min and the mixture was then stirred at this temperature for 30 min. Thereafter, methanol (15 ml) was added dropwise such that the internal temperature remained at −78° C., before the mixture was then slowly warmed to room temperature. Saturated sodium chloride solution (20 ml) was added to the reaction mixture and the suspension was filtered through sea sand. The organic phase was dried with sodium sulfate and concentrated i. vac. The residue was purified by flash chromatography with cyclohexane/ethyl acetate (1:3).

후처리

  1. customremained at −78° C., before the mixture
  2. filtrationthe suspension was filtered through sea sand
  3. dry with materialThe organic phase was dried with sodium sulfate
  4. concentrationconcentrated i
  5. customThe residue was purified by flash chromatography with cyclohexane/ethyl acetate (1:3)

출처 및 근거

ORD 기록
ord-bb27e75eb7a647f39d22d5a4043b3d73
출처 데이터셋
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08106055B2

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