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2-(Phenoxazin-10-yl)ethyl methanesulfonate → Ethyl 3-[4-[2-(phenoxazin-10-yl)ethoxy]phenyl]-2-butoxypropanoate

HRID 1243816
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반응식

HRID 1243816 반응식
CS([O:5][CH2:6][CH2:7][N:8]1[C:21]2[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=2[O:15][C:14]2[C:9]1=[CH:10][CH:11]=[CH:12][CH:13]=2)(=O)=O.[CH2:22]([O:26][CH:27]([CH2:33][C:34]1[CH:39]=[CH:38][C:37](O)=[CH:36][CH:35]=1)[C:28]([O:30][CH2:31][CH3:32])=[O:29])[CH2:23][CH2:24][CH3:25]>>[CH:20]1[C:21]2[N:8]([CH2:7][CH2:6][O:5][C:37]3[CH:36]=[CH:35][C:34]([CH2:33][CH:27]([O:26][CH2:22][CH2:23][CH2:24][CH3:25])[C:28]([O:30][CH2:31][CH3:32])=[O:29])=[CH:39][CH:38]=3)[C:9]3[C:14](=[CH:13][CH:12]=[CH:11][CH:10]=3)[O:15][C:16]=2[CH:17]=[CH:18][CH:19]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 112204632-(Phenoxazin-10-yl)ethyl methanesulfonateHCID 21930975Ethyl 2-butoxy-3-(4-hydroxyphenyl)propanoate

생성물 1

HCID 9934654Ethyl 3-[4-[2-(phenoxazin-10-yl)ethoxy]phenyl]-2-butoxypropanoate수율 54.2%

실험 절차

The title compound (0.25 g, 53%) was prepared as a colorless liquid from 2-(phenoxazin-10-yl)ethyl methanesulfonate (0.3 g, 0.98 mmol) and ethyl 2-butoxy-3-(4-hydroxyphenyl)propanoate (0.26 g, 0.97 mmol) obtained in preparation 6 by an analogous procedure to that described in example 6 (Method B).

후처리

  1. customobtained in preparation 6 by an analogous procedure to

출처 및 근거

ORD 기록
ord-c02a2cd2648a4f2091e2b2ded74b033a
출처 데이터셋
uspto-grants-2006_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07119198B2

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