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2,6-Lutidine → 3,5-Dibromosalicyl 3-butenoate

HRID 567667
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HRID 567667 반응식
[C:1](Cl)(=[O:5])[CH2:2][CH:3]=[CH2:4].[Br:7][C:8]1[CH:16]=[C:15]([Br:17])[CH:14]=[C:10]([C:11]([OH:13])=O)[C:9]=1[OH:18].N1C(C)=CC=CC=1C>CC(C)=O>[C:1]([O:13][CH2:11][C:10]1[C:9](=[C:8]([Br:7])[CH:16]=[C:15]([Br:17])[CH:14]=1)[OH:18])(=[O:5])[CH2:2][CH:3]=[CH2:4]
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참가 물질

5

반응물 3

HCID 79372,6-LutidineHCID 184643,5-Dibromosalicylic acidHCID 10975427But-3-enoyl Chloride

생성물 1

HCID 212622063,5-Dibromosalicyl 3-butenoate

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

3,5-Dibromosalicyl 3-butenoate is prepared by reaction of an acetone solution of 3-butenoyl chloride and 3,5-dibromosalicylic acid in the presence of 2,6-lutidine. The 3-butenoate ester is isolated and purified. In a second step, the desired oxirane, 3,5-dibromosalicyl 3,4-oxabutanoate, is prepared by reaction of 3,5-dibromosalicyl 3-butenoate and 3-chloroperbenzoic acid in chloroform solution. The desired oxirane is isolated and purified.

출처 및 근거

ORD 기록
ord-137ef8ba307b4b909a8d6201c4b20be9
출처 데이터셋
uspto-grants-2001_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06180598B2

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