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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 20310988, 화합물 → HCID 20310959, 화합물

HRID 1763695
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인쇄 미리보기

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HRID 1763695 반응식
ClCCCC(OC(=O)C)CCCCCCC.BrCC=CC(OC(=O)C)CCCCC.C([O:34][CH:35]([CH2:58][CH2:59][CH2:60][CH2:61][CH2:62][CH2:63][CH3:64])[CH2:36][CH2:37][CH2:38][N:39]([CH2:44][CH2:45][CH2:46][C:47]1[CH:57]=[CH:56][C:50]([C:51]([O:53]CC)=[O:52])=[CH:49][CH:48]=1)[S:40]([CH3:43])(=[O:42])=[O:41])(=O)C>>[OH:34][CH:35]([CH2:58][CH2:59][CH2:60][CH2:61][CH2:62][CH2:63][CH3:64])[CH2:36][CH2:37][CH2:38][N:39]([CH2:44][CH2:45][CH2:46][C:47]1[CH:57]=[CH:56][C:50]([C:51]([OH:53])=[O:52])=[CH:49][CH:48]=1)[S:40]([CH3:43])(=[O:41])=[O:42]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 20310988HCID 20310988, 화합물HCID 203860511-Chloro-4-acetoxyundecaneHCID 540485691-Bromo-4-acetoxy-2-nonene

생성물 1

HCID 20310959HCID 20310959, 화합물

실험 절차

This compound is prepared by the series of reactions described in Example 3, except that in Step B an equivalent amount of 1-chloro-4-acetoxyundecane is substituted for 1-bromo-4-acetoxy-2-nonene and the heating period at 90° C. is extended to 28 hours. There is thus obtained in Step B of this example, ethyl 4-{3-[N-(4-acetoxyundecyl)methanesulfonamido]propyl}benzoate. Saponficiation of this ester is STep C yields 4-{3-[N-(4-hydroxyundecyl)methanesulfonamido]propyl}benzoic acid.

후처리

custom
This compound is prepared by the series of reactions

출처 및 근거

ORD 기록
ord-fd1a84e00cc545cbb636be6ef90eafbf
출처 데이터셋
uspto-grants-1978_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04112236

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