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Sodium Hydroxide → 4-(Chloro(4-chlorophenyl)methyl)-1-methylpiperidine

HRID 1443039
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HRID 1443039 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([CH:10]2[CH2:15][CH2:14][N:13]([CH3:16])[CH2:12][CH2:11]2)O)=[CH:4][CH:3]=1.S(Cl)([Cl:19])=O.[OH-].[Na+]>C1(C)C=CC=CC=1>[Cl:19][CH:8]([C:5]1[CH:6]=[CH:7][C:2]([Cl:1])=[CH:3][CH:4]=1)[CH:10]1[CH2:15][CH2:14][N:13]([CH3:16])[CH2:12][CH2:11]1
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참가 물질

5

반응물 3

HCID 14798Sodium HydroxideHCID 24386Thionyl ChlorideHCID 541856alpha-[4-Chlorophenyl]-1-methyl-4-piperidinemethanol

생성물 1

HCID 597169334-(Chloro(4-chlorophenyl)methyl)-1-methylpiperidine

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

To a solution of 4-chlorophenyl 1-methylpiperidin-4-yl methanol 1.2 g (5.02 mmol) in toluene (5 ml) was added thionyl chloride (0.45 ml) dropwise. The resulting mixture was stirred at room temperature over night. The mixture was then made alkaline with NaOH solution and extracted with ethyl acetate (3×40). The combined organic solution was dried and concentrated to give 1.2 g of desired product.

후처리

  1. extractionextracted with ethyl acetate (3×40)
  2. customThe combined organic solution was dried
  3. concentrationconcentrated

출처 및 근거

ORD 기록
ord-041276996f234298a025d98ae4560f94
출처 데이터셋
uspto-grants-2010_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07659395B2

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