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2-Bromopropane → HCID 59419921, 화합물

HRID 587917
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HRID 587917 반응식
[CH2:1]([O:3][C:4](=[O:16])[CH2:5][C:6]1[CH:11]=[CH:10][C:9]([O:12][CH3:13])=[C:8]([O:14][CH3:15])[CH:7]=1)[CH3:2].CO[C:19]1C=C(CC#N)C=[CH:23][C:24]=1OC.Cl[C:31]([O:33][CH2:34][CH3:35])=[O:32].[Br:36]C(C)C.C([N-]C(C)C)(C)C.[Li+].C[Si]([N-][Si](C)(C)C)(C)C.[Na+].[H-].[Na+]>>[Br:36][CH2:23][CH2:24][CH2:19][C:5]([C:6]1[CH:11]=[CH:10][C:9]([O:12][CH3:13])=[C:8]([O:14][CH3:15])[CH:7]=1)([C:31]([O:33][CH2:34][CH3:35])=[O:32])[C:4]([O:3][CH2:1][CH3:2])=[O:16]
참가 물질실험 절차출처 및 근거반응 노트

참가 물질

8

반응물 7

HCID 63582-BromopropaneHCID 10928Ethyl chloroformateHCID 24758Sodium hydrideHCID 667273,4-DimethoxybenzeneacetonitrileHCID 87441Ethyl 3,4-dimethoxyphenylacetateHCID 2724254Sodium bis(trimethylsilyl)amide2회HCID 2724682Lithium diisopropylamide

생성물 1

HCID 59419921HCID 59419921, 화합물

실험 절차

For Step 1, (3,4-dimethoxy-phenyl)-acetic acid ethyl ester was substituted for (3,4-Dimethoxyphenyl)acetonitrile, ethyl chloroformate was substituted for 2-bromopropane and lithium diisopropylamide (LDA) was substituted for NaHMDS. For Step 2, sodium hydride was substituted for NaHMDS.

출처 및 근거

ORD 기록
ord-fe273c7d3ece4bedade145579cbc2a75
출처 데이터셋
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09227918B2

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