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Sodium Hydroxide → 4-Boc-2-methyl-1-phenylpiperazine

HRID 2416656
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HRID 2416656 반응식
[CH3:1][CH:2]1[N:7]([C:8]2[CH:13]=[CH:12][C:11](N)=[CH:10][CH:9]=2)[CH2:6][CH2:5][N:4]([C:15]([O:17][C:18]([CH3:21])([CH3:20])[CH3:19])=[O:16])[CH2:3]1.N([O-])=O.[Na+].[OH-].[Na+]>[PH2](O)=O.O.[Cu-]=O>[CH3:1][CH:2]1[N:7]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH2:6][CH2:5][N:4]([C:15]([O:17][C:18]([CH3:19])([CH3:21])[CH3:20])=[O:16])[CH2:3]1
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참가 물질

7

반응물 3

HCID 14798Sodium HydroxideHCID 22633057(+/-)-tert-Butyl 3-methyl-4-(4-aminophenyl)piperazine-1-carboxylateHCID 23668193Sodium Nitrite

생성물 1

HCID 226330714-Boc-2-methyl-1-phenylpiperazine

시약·촉매·용매 3

HCID 178419072HCID 178419072, 화합물촉매HCID 962Water
용매
HCID 4124402Phosphinic Acid용매

실험 절차

To a solution of (±)-tert-butyl 3-methyl-4-(4-aminophenyl)piperazine-1-carboxylate (325 mg) in 50% hypophosphorous acid (1.27 ml) containing copper(I) oxide (8.0 mg) was added dropwise a solution of sodium nitrite (92 mg) in water (2 ml) at 0° C. with stirring. After 2 hours, the reaction mixture was made alkaline with 40% NaOH solution and extracted with ethyl acetate twice. The organic layers were combined and washed with water and brine. The solvent was evaporated, and the residue was purified by silica gel column chromatography (hexane-ethyl acetate 1:1) to give the title compound in a pure form as colorless oil.

후처리

  1. extractionextracted with ethyl acetate twice
  2. washwashed with water and brine
  3. customThe solvent was evaporated
  4. customthe residue was purified by silica gel column chromatography (hexane-ethyl acetate 1:1)

출처 및 근거

ORD 기록
ord-af3dad8bbe5a48e8995131070a264a16
출처 데이터셋
uspto-grants-2004_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06825200B1

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