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HCID 21996962, 화합물 → HCID 70149291, 화합물

HRID 1976326
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HRID 1976326 반응식
BrC1C=[CH:6][C:5]([O:8]C(C)C)=[C:4](C(C2C=CC(C)=CC=2)=C)C=1.BrC1C=CC(CC(=O)C)=C(C(C2C=CC(C)=CC=2)=C)C=1.[Br:41][C:42]1[CH:47]=[CH:46][C:45]([OH:48])=[C:44]([C:49]([C:51]2[CH:52]=[C:53]([CH3:57])[CH:54]=[CH:55][CH:56]=2)=[CH2:50])[CH:43]=1>>[Br:41][C:42]1[CH:47]=[CH:46][C:45]([O:8][CH:5]([CH3:6])[CH3:4])([OH:48])[CH:44]([C:49]([C:51]2[CH:52]=[C:53]([CH3:57])[CH:54]=[CH:55][CH:56]=2)=[CH2:50])[CH:43]=1
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HCID 21996962HCID 21996962, 화합물2회HCID 21996984HCID 21996984, 화합물HCID 131722536HCID 131722536, 화합물

생성물 1

HCID 70149291HCID 70149291, 화합물

실험 절차

Employing the same general procedure as for the preparation of 4-bromo-1-isopropoxy-2-[(1-p-tolyl)vinyl]benzene (Compound S), 81.5 mg (0.3 mmol) of 4-bromo-2-[(1-m-tolyl)vinyl]phenol (Compound N) was converted into the title compound using 164 mg (0.6 mmol) of triphenylphosphine, 0.10 mL (108 mg, 0.6 mmol) of diethylazodicarboxylate, 0.05 mL (39 mg, 0.6 mmol) of isopropanol and 3 mL of tetrahydrofuran. The reaction was sluggish necessitating addition (after 23 hours of stirring at ambient temperature) of another equivalent of reagents (initially only 1/2 of the above amounts were added) and stirring for 4 additional days. Purification by flash chromatography (silica, 10% ethyl acetate in hexane) gave the title compound as a pink oil.

출처 및 근거

ORD 기록
ord-b50355578ad843ebb669dcc4086c0b24
출처 데이터셋
uspto-grants-2001_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06225494B1

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