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1-Chloro-2-nitrobenzene → 4-[(2-Nitrophenoxy)methyl]piperidine

HRID 1389242
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HRID 1389242 반응식
[OH:1][CH2:2][CH:3]1[CH2:8][CH2:7][NH:6][CH2:5][CH2:4]1.Cl[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=1[N+:16]([O-:18])=[O:17].[OH-].[K+]>O1CCOCC1>[N+:16]([C:11]1[CH:12]=[CH:13][CH:14]=[CH:15][C:10]=1[O:1][CH2:2][CH:3]1[CH2:8][CH2:7][NH:6][CH2:5][CH2:4]1)([O-:18])=[O:17]
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참가 물질

5

반응물 3

HCID 69451-Chloro-2-nitrobenzeneHCID 14797Potassium HydroxideHCID 4207714-Piperidinemethanol

생성물 1

HCID 202988744-[(2-Nitrophenoxy)methyl]piperidine수율 22.2%

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

반응 조건

온도
70 °C

실험 절차

A mixture of 23.0 g (0.2 mole) of 4-hydroxymethylpiperidine, 31.5 g (0.2 mole) of 2-chloronitrobenzene, 11.8 g (0.21 mole) of potassium hydroxide and 200 ml of dioxane is heated to 70° C. for 3 days. The reaction mixture is then evaporated in a vacuum and the residue is taken up in diethyl ether, washed with water, extracted with dilute hydrochloric acid, rendered alkaline and the aqueous mixture extracted with diethyl ether. After evaporation of the solvent, there are obtained 10.5 g of 4-(2-nitrophenoxymethyl)-piperidine (22% of theory); b.p. 130°-132° C./0.01 mm. Hg.

후처리

  1. customThe reaction mixture is then evaporated in a vacuum
  2. washwashed with water
  3. extractionextracted with dilute hydrochloric acid
  4. extractionthe aqueous mixture extracted with diethyl ether
  5. customAfter evaporation of the solvent, there

출처 및 근거

ORD 기록
ord-7c95348764444583b21e444d0cd92f7c
출처 데이터셋
uspto-grants-1981_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04243807

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