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Acetic acid, ion(1-) (8CI,9CI) → 5-甲基-吡啶-2-基)甲醇

HRID 369652
笔记
打印预览

反应方程式

HRID 369652 反应方程式
C([O:4][CH2:5][C:6]1[CH:11]=[CH:10][C:9]([CH3:12])=[CH:8][N:7]=1)(=O)C.C(N(CC)CC)C.C(OCC)(=O)C.C([O-])(=O)C>Cl>[OH:4][CH2:5][C:6]1[CH:11]=[CH:10][C:9]([CH3:12])=[CH:8][N:7]=1
参与物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 175Acetic acid, ion(1-) (8CI,9CI)HCID 8471三乙胺HCID 8857乙酸乙酯HCID 123253842-acetoxymethyl-5-methyl pyridine

产物 1

HCID 123253875-甲基-吡啶-2-基)甲醇收率 84%

试剂、催化剂与溶剂 1

HCID 313盐酸溶剂

实验过程

2-Acetoxymethyl-5-methyl pyridine (30 g, 182 mmol) was dissolved in hydrochloric acid (100 mL, 4 N). The mixture was heated under reflux, until TLC (silica gel; triethylamine:ethyl acetate:petroleum ether 40-60=1:9:19) showed complete absence of the acetate (normally 1 hour). The mixture was cooled, brought to pH>11, extracted with dichloromethane (3×50 mL) and the solvent removed in vacuo. Pure 2-hydroxymethyl-5-methyl pyridine (18.80 g, 152 mmol, 84%) was obtained by Kugelrohr distillation (p=20 mm Hg, T=130° C.) as a slightly yellow oil.

后处理

  1. temperatureThe mixture was heated
  2. customnormally 1 hour
  3. temperatureThe mixture was cooled
  4. extractionextracted with dichloromethane (3×50 mL)
  5. customthe solvent removed in vacuo

来源与证据

ORD记录
ord-b971476841dd4042aa7782cc9397a8e2
来源数据集
uspto-grants-2000_10
DOI
10.6084/m9.figshare.5104873.v1
专利号
US06140294

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