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Tributylvinyltin → HCID 67517397, 화합물

HRID 2173441
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HRID 2173441 반응식
Br[C:2]1[CH:7]=[C:6]([N:8]2[CH:12]=[N:11][N:10]=[N:9]2)[CH:5]=[CH:4][C:3]=1[CH2:13][C:14]([OH:16])=[O:15].[Li+].[Cl-].[CH2:19]=[CH:20][Sn](CCCC)(CCCC)CCCC>C1(C)C=CC=CC=1.CCOC(C)=O.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[CH:19]([C:2]1[CH:7]=[C:6]([N:8]2[CH:12]=[N:11][N:10]=[N:9]2)[CH:5]=[CH:4][C:3]=1[CH2:13][C:14]([OH:16])=[O:15])=[CH2:20]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 3

HCID 81998TributylvinyltinHCID 433294Lithium ChlorideHCID 67517645HCID 67517645, 화합물

생성물 1

HCID 67517397HCID 67517397, 화합물

시약·촉매·용매 3

HCID 178418397HCID 178418397, 화합물촉매HCID 1140Toluene용매
HCID 8857
Ethyl Acetate
용매

실험 절차

To a solution of [2-bromo-4-(1H-tetrazol-1-yl)phenyl]acetic acid (100 mg, 0.35 mmol) in 10 mL of toluene was added LiCl (44 mg, 1.05 mmol), Pd(PPh3)4(10 mg), CH2═CHSnBu3 (222 mg, 0.7 mmol), and the mixture was heated to reflux overnight. After the reaction was completed, the reaction solution was diluted with EtOAc and filtered. The filtrate was concentrated and purified by prep-TLC to give [2-ethenyl-4-(1H-tetrazol-1-yl)phenyl]acetic acid.

후처리

  1. temperaturethe mixture was heated
  2. temperatureto reflux overnight
  3. filtrationfiltered
  4. concentrationThe filtrate was concentrated
  5. custompurified by prep-TLC

출처 및 근거

ORD 기록
ord-1e09d4bde36d4e618ce26b2e6535bb1f
출처 데이터셋
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09056859B2

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