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三丁基氯化锡 → 4-三丁基锡烷基-3,5-二甲基异恶唑

HRID 1410129
笔记
打印预览

反应方程式

HRID 1410129 反应方程式
[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
参与物实验过程后处理来源与证据反应笔记

参与物

5

反应物 3

HCID 15096三丁基氯化锡HCID 6138833,5-二甲基-4-碘基异噁唑HCID 178418339正丁基锂

产物 1

HCID 150622154-三丁基锡烷基-3,5-二甲基异恶唑收率 39.2%

试剂、催化剂与溶剂 1

HCID 8028四氢呋喃溶剂

实验过程

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%).

后处理

  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)

来源与证据

ORD记录
ord-40ad9d906b3b4c51acc6df0bdb45cdc1
来源数据集
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
专利号
US08921402B2

反应笔记

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本页导航参与物实验过程后处理来源与证据反应笔记