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Tributyltin Chloride → 3,5-Dimethyl-4-(tributylstannyl)isoxazole

HRID 1410129
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HRID 1410129 반응식
[Li]CCCC.I[C:7]1[C:8]([CH3:13])=[N:9][O:10][C:11]=1[CH3:12].[CH2:14]([Sn:18](Cl)([CH2:23][CH2:24][CH2:25][CH3:26])[CH2:19][CH2:20][CH2:21][CH3:22])[CH2:15][CH2:16][CH3:17]>C1COCC1>[CH3:13][C:8]1[C:7]([Sn:18]([CH2:19][CH2:20][CH2:21][CH3:22])([CH2:23][CH2:24][CH2:25][CH3:26])[CH2:14][CH2:15][CH2:16][CH3:17])=[C:11]([CH3:12])[O:10][N:9]=1
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참가 물질

5

반응물 3

HCID 15096Tributyltin ChlorideHCID 6138834-Iodo-3,5-dimethyl-1,2-oxazoleHCID 178418339Butyllithium

생성물 1

HCID 150622153,5-Dimethyl-4-(tributylstannyl)isoxazole수율 39.2%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

n-BuLi (1.6 M solution in hexanes, 6 mL, 9.6 mmol) was added to a cooled (−78° C.) solution of 4-iodo-3,5-dimethylisoxazole (1.47 g, 6.60 mmol) in THF (24 mL) under nitrogen. After 15 min, tributyltin chloride (26 mL, 9.60 mmol) was added and the reaction was stirred over night while warming to room temperature. The reaction was quenched by 1 M HCl, CH2Cl2 was added, the phases separated and the solvent were evaporated. The residue was purified by flash chromatography with heptane: CH2Cl2 (75:25-0:100) to give 3,5-dimethyl-4-(tributylstannyl)isoxazole (1.00 g, 39%).

후처리

  1. customThe reaction was quenched by 1 M HCl, CH2Cl2
  2. additionwas added
  3. customthe phases separated
  4. customthe solvent were evaporated
  5. customThe residue was purified by flash chromatography with heptane: CH2Cl2 (75:25-0:100)

출처 및 근거

ORD 기록
ord-40ad9d906b3b4c51acc6df0bdb45cdc1
출처 데이터셋
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08921402B2

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