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Phenethylamine → Methyl 7-[(2-phenylethyl)amino]heptanoate

HRID 1080543
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반응식

HRID 1080543 반응식
[C:1]1([CH2:7][CH2:8][NH2:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C(N(CC)CC)C.Br[CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][C:24]([O:26][CH3:27])=[O:25]>C1(C)C=CC=CC=1>[C:1]1([CH2:7][CH2:8][NH:9][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][C:24]([O:26][CH3:27])=[O:25])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
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참가 물질

5

반응물 3

HCID 1001PhenethylamineHCID 8471TriethylamineHCID 554086Methyl 7-bromoheptanoate

생성물 1

HCID 19047852Methyl 7-[(2-phenylethyl)amino]heptanoate수율 26.2%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

To a mixture of 2-phenylethylamine (1.09 g, 9 mmol) and triethylamine (1.37 g, 13.5 mmol) in toluene (50 mL) was added methyl 7-bromoheptanoate (2.0 g, 9 mmol) and refluxed overnight. The reaction mixture was filtered and concentrated. Flash column chromatography over silica gel using 100% ethyl acetate yielded a yellow oil (0.62 g, 20%) NMR (250 MHz, CDCl3), 1.12-1.40 (4H, m), 1.40-1.72 (4H, m), 2.29 (2H, t), 2.63 (2H, t), 2.75-2.96 (4H, m), 2.96-3.1 (1H, br s), 3.66 (3H, s), 7.00-7.38 (5H, m).

후처리

  1. temperaturerefluxed overnight
  2. filtrationThe reaction mixture was filtered
  3. concentrationconcentrated

출처 및 근거

ORD 기록
ord-e95dfc1554da448ea3cbc270fedb5d36
출처 데이터셋
uspto-grants-1996_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05580896

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