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2-Fluorotoluene → 1-Benzyl-4-(o-tolyloxy)piperidine

HRID 437554
노트
인쇄 미리보기

반응식

HRID 437554 반응식
[CH2:1]([N:8]1[CH2:13][CH2:12][CH:11]([OH:14])[CH2:10][CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.F[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=1[CH3:22]>>[CH2:1]([N:8]1[CH2:13][CH2:12][CH:11]([O:14][C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=2[CH3:22])[CH2:10][CH2:9]1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 72412-FluorotolueneHCID 784611-Benzylpiperidin-4-ol

생성물 1

HCID 214287021-Benzyl-4-(o-tolyloxy)piperidine

실험 절차

By following the manipulative procedure described in Example 1(a), 21.0 g of 1-benzyl-4-piperidinol and 24.0 g of o-fluorotoluene produces a yellow oil fraction which boils at 161°-163° C., 0.09 mm. This oil solidifies slowly upon standing and is recrystallized from petroleum ether (b.p. 30°-60°) to give white crystals of 1-benzyl-4-(o-tolyloxy) piperidine.

후처리

  1. customproduces a yellow oil fraction which boils at 161°-163° C., 0.09 mm
  2. customis recrystallized from petroleum ether (b.p. 30°-60°)

출처 및 근거

ORD 기록
ord-37c52c96522c47929cc932db7d422f4b
출처 데이터셋
uspto-grants-1977_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04031221

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