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Triphenylphosphine → 4-(1-t-Butoxycarbonylpiperidin-4-yloxy)-3-chloronitrobenzene

HRID 1796196
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HRID 1796196 반응식
[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][CH:11]([OH:14])[CH2:10][CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[Cl:15][C:16]1[CH:21]=[C:20]([N+:22]([O-:24])=[O:23])[CH:19]=[CH:18][C:17]=1O.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>ClCCl.N(C(OCC)=O)=NC(OCC)=O>[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][CH:11]([O:14][C:17]2[CH:18]=[CH:19][C:20]([N+:22]([O-:24])=[O:23])=[CH:21][C:16]=2[Cl:15])[CH2:10][CH2:9]1)=[O:7])([CH3:4])([CH3:2])[CH3:3]
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참가 물질

6

반응물 3

HCID 11776TriphenylphosphineHCID 12074NitrofunginHCID 643502Tert-butyl 4-hydroxypiperidine-1-carboxylate

생성물 1

HCID 221810984-(1-t-Butoxycarbonylpiperidin-4-yloxy)-3-chloronitrobenzene수율 80.4%

시약·촉매·용매 2

HCID 6344Dichloromethane용매
HCID 220568
ethyl N-ethoxycarbonyliminocarbamate
용매

실험 절차

To a solution of 1-t-butoxycarbonyl-4-hydroxypiperidine (3.32 g), 2-chloro-4-nitrophenol (2.36 g) and triphenylphosphine (5.11 g) in dichloromethane (60 ml), diethyl azodicarboxylate (3.10 ml) was added dropwise with stirring under ice-cooling, and the resulting mixture was stirred at room temperature for 18 hours and then evaporated in vacuo. The residue obtained was purified by chromatography on a silica gel column using a mixed solvent of hexane and ethyl acetate (5:2) as the eluent to afford the title compound (3.90 g, yield: 76%) as a pale yellow solid.

후처리

  1. temperaturecooling
  2. stirringthe resulting mixture was stirred at room temperature for 18 hours
  3. customevaporated in vacuo
  4. customThe residue obtained
  5. customwas purified by chromatography on a silica gel column

출처 및 근거

ORD 기록
ord-1e3a748eb73f4746ba9214dced3c8128
출처 데이터셋
uspto-grants-2006_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07030138B2

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