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Triethylamine → HCID 19096826, 화합물

HRID 486986
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HRID 486986 반응식
Cl[C:2]([C:4]1([C:9]([O:11][CH2:12][CH3:13])=[O:10])[CH2:8][CH2:7][CH2:6][CH2:5]1)=[O:3].[Br:14][C:15]1[CH:21]=[CH:20][C:18]([NH2:19])=[C:17]([CH3:22])[CH:16]=1.C(N(CC)CC)C>O1CCCC1>[Br:14][C:15]1[CH:21]=[CH:20][C:18]([NH:19][C:2]([C:4]2([C:9]([O:11][CH2:12][CH3:13])=[O:10])[CH2:8][CH2:7][CH2:6][CH2:5]2)=[O:3])=[C:17]([CH3:22])[CH:16]=1
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5

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HCID 8471TriethylamineHCID 114234-Bromo-2-methylanilineHCID 19096799Ethyl 1-(chlorocarbonyl)cyclopentane-1-carboxylate

생성물 1

HCID 19096826HCID 19096826, 화합물수율 35%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

Ethyl 1-chlorocarbonylcyclopentanecarboxylate (3.10 grams, 0.02 mole) prepared in Example XX, 4-bromo-2-methylaniline (2.82 grams, 0.02 mole) and triethylamine (1.53 grams, 0.02 mole) were reacted in tetrahydrofuran (200 milliliters) under conditions similar to those described in Example I to give 2.40 grams (0.007 mole) of ethyl 1-(4-bromo-2-methylphenylaminocarbonyl)cyclopentanecarboxylate which, after recrystallization from hexane, had a melting point of 64° C.-67° C. Elemental analysis of the product indicated the following:

출처 및 근거

ORD 기록
ord-0d0c87a41b3242bc9ef6820b31716d3b
출처 데이터셋
uspto-grants-1994_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05292937

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