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聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯] → 1-Fluoroethvlbenzimidazole

HRID 2231237
笔记
打印预览

反应方程式

HRID 2231237 反应方程式
O[CH:2]([C:4]1[NH:5][C:6]2[CH:12]=[CH:11][CH:10]=[CH:9][C:7]=2[N:8]=1)[CH3:3].C(N(S(F)(F)[F:19])CC)C.O.[OH-].[Na+]>C(Cl)Cl>[F:19][CH:2]([C:4]1[NH:5][C:6]2[CH:12]=[CH:11][CH:10]=[CH:9][C:7]=2[N:8]=1)[CH3:3]
参与物反应条件实验过程后处理来源与证据反应笔记

参与物

6

反应物 4

HCID 962聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯]HCID 14798氢氧化钠HCID 123472二乙胺基三氟化硫(DAST)HCID 2059222-(1-羟乙基)苯并咪唑

产物 1

HCID 538247831-Fluoroethvlbenzimidazole收率 38.1%

试剂、催化剂与溶剂 1

HCID 6344二氯甲烷溶剂2 次

反应条件

温度
-78 °C

实验过程

A solution of 3.24 g (0.02 mole) of 1-hydroxyethylbenzimidazole in 50 ml of methylene chloride was added to a solution of 2.44 ml (0.02 mole) of diethylaminosulfur trifluoride in 50 ml of methylene chloride cooled to -78° C. and under a nitrogen atmosphere. The reaction mixture was allowed to warm slowly to room temperature where it was stirred for 4 hours. The mixture was poured into water, the pH adjusted to 8 with aqueous sodium hydroxide solution and the organic layer separated and dried. Removal of the solvent gave 1.25 g of a brown oil which was chromatographed on 100 g of silica gel using 5% methanol chloroform as the eluent, 845 mg.

后处理

  1. temperatureto warm slowly to room temperature where it
  2. customthe organic layer separated
  3. customdried
  4. customRemoval of the solvent

来源与证据

ORD记录
ord-dd2fc4b3387d4ce39a2ef7faa0ce19b6
来源数据集
uspto-grants-1988_11
DOI
10.6084/m9.figshare.5104873.v1
专利号
US04782050

反应笔记

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本页导航参与物反应条件实验过程后处理来源与证据反应笔记