化工社
首页MCP工作台Skills
首页工作台通知我的
llms.txt · MCP 指南隐私政策 · 服务条款 · 支持v1.8.0
  1. 首页
  2. /反应

三乙胺 → 5-(2-Methylbenzoyloxy)indan

HRID 36932
笔记
打印预览

反应方程式

HRID 36932 反应方程式
[OH:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[CH2:7][CH2:6][CH2:5]2.C(N(CC)CC)C.[CH3:18][C:19]1[CH:27]=[CH:26][CH:25]=[CH:24][C:20]=1[C:21](Cl)=[O:22]>ClCCl>[CH3:18][C:19]1[CH:27]=[CH:26][CH:25]=[CH:24][C:20]=1[C:21]([O:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[CH2:7][CH2:6][CH2:5]2)=[O:22]
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 8471三乙胺HCID 151185-茚醇HCID 70276methylbenzoyl chloride

产物 1

HCID 99923955-(2-Methylbenzoyloxy)indan

试剂、催化剂与溶剂 1

HCID 6344二氯甲烷溶剂

实验过程

To an ice-cooled mixture of 5-hydroxyindan (13.4 g), triethylamine (14.0 ml) and dichloromethane (150 ml) was added 2-methylbenzoyl chloride (15.4 ml) dropwise with constant stirring. The mixture was further stirred under ice-cooling for one hour, after which it was washed with water and dried (MgSO4). The solvent was then distilled off to give 5-(2-methylbenzoyloxy)indan as oil in quantitative yield.

后处理

  1. temperaturecooling for one hour
  2. washafter which it was washed with water
  3. dry with materialdried (MgSO4)
  4. distillationThe solvent was then distilled off

来源与证据

ORD记录
ord-4a2639ed63af4ae696074f62c7fedcef
来源数据集
uspto-grants-1995_05
DOI
10.6084/m9.figshare.5104873.v1
专利号
US05418239

反应笔记

加载中…

本页导航参与物实验过程后处理来源与证据反应笔记