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Methyl 4-bromo-2-nitrobenzoate → 2-Nitro-4-vinyl-benzoic acid methyl ester

HRID 1441624
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HRID 1441624 반응식
[CH3:1][O:2][C:3](=[O:14])[C:4]1[CH:9]=[CH:8][C:7](Br)=[CH:6][C:5]=1[N+:11]([O-:13])=[O:12].[CH2:15](C([Sn])=C(CCCC)CCCC)[CH2:16]CC>O1CCOCC1.CCOC(C)=O.Cl[Pd](Cl)([P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1>[CH3:1][O:2][C:3](=[O:14])[C:4]1[CH:9]=[CH:8][C:7]([CH:15]=[CH2:16])=[CH:6][C:5]=1[N+:11]([O-:13])=[O:12]
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참가 물질

6

반응물 2

HCID 18350461Methyl 4-bromo-2-nitrobenzoateHCID 53438229Tri(butyl)vinyltin

생성물 1

HCID 591644672-Nitro-4-vinyl-benzoic acid methyl ester수율 102.8%

시약·촉매·용매 3

HCID 178418476HCID 178418476, 화합물촉매HCID 8857Ethyl Acetate용매
HCID 31275
1,4-Dioxane
용매

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온도
80 °C

실험 절차

To a solution of 4-bromo-2-nitro-benzoic acid methyl ester (1 g, 3.85 mmol) in dioxane (5 mL) were added tributylvinyltin (1.7 mL, 5.76 mmol) and Pd(Ph3P)2Cl2 (275.4 mg, 0.385 mmol). The reaction mixture was stirred at 80° C. for 18 h, was cooled to r.t. and was diluted with EtOAc. After removal of the precipitate by filtration, the solution was concentrated in vacuo. The residue was purified by flash chromatography (silica gel, hexanes 1:1 hexanes:EtOAc) to provide the title compound (820 mg, 100%, 97% purity by HPLC) as a yellow oil. ESI-MS: m/z 208.2 [M+H]+, rt 5.14 min.

후처리

  1. temperaturewas cooled to r.t.
  2. customAfter removal of the precipitate
  3. filtrationby filtration
  4. concentrationthe solution was concentrated in vacuo
  5. customThe residue was purified by flash chromatography (silica gel, hexanes 1:1 hexanes:EtOAc)

출처 및 근거

ORD 기록
ord-7a76e81ad050402b963b34fccfd6ebbc
출처 데이터셋
uspto-grants-2010_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07655666B2

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