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Hydrogen Bromide → HCID 58372746, 화합물

HRID 888519
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HRID 888519 반응식
C([O:3][C:4](=[O:31])[CH2:5][C:6]1[CH:11]=[CH:10][C:9]([O:12]C)=[C:8]([O:14][C:15]2[CH:20]=[CH:19][C:18]([N+:21]([O-:23])=[O:22])=[CH:17][C:16]=2[CH2:24][S:25][CH2:26][C:27]([F:30])([F:29])[F:28])[CH:7]=1)C.Br>C(O)(=O)C>[OH:12][C:9]1[CH:10]=[CH:11][C:6]([CH2:5][C:4]([OH:31])=[O:3])=[CH:7][C:8]=1[O:14][C:15]1[CH:20]=[CH:19][C:18]([N+:21]([O-:23])=[O:22])=[CH:17][C:16]=1[CH2:24][S:25][CH2:26][C:27]([F:30])([F:28])[F:29]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 260Hydrogen BromideHCID 58372816HCID 58372816, 화합물

생성물 1

HCID 58372746HCID 58372746, 화합물

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

{4-Methoxy-3-[4-nitro-2-(2,2,2-trifluoro-ethylsulfanylmethyl)-phenoxy]-phenyl}-acetic acid ethyl ester (1.5 g, 3.6 mmol) was treated with 48% hydrogen bromide in acetic acid (1:1; 20 mL) at 100° C. overnight. After work-up with EtOAc and H2O, the crude material was purified by preparative HPLC to give {4-hydroxy-3-[4-nitro-2-(2,2,2-trifluoro-ethylsulfanylmethyl)-phenoxy]-phenyl}-acetic acid.

후처리

  1. custom
After work-up with EtOAc and H2O, the crude material was purified by preparative HPLC

출처 및 근거

ORD 기록
ord-98f67bc8b3884edea6f9863cc13b80c1
출처 데이터셋
uspto-grants-2012_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08247602B2

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