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聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯] → 2-cyclopropyl-5-hydroxy-1-(phenylmethyl)-1H-indole-3-acetamide

HRID 1069644
笔记
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反应方程式

HRID 1069644 反应方程式
[CH:1]1([C:4]2[N:5]([CH2:19][C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=3)[C:6]3[C:11]([C:12]=2[CH2:13][C:14]([NH2:16])=[O:15])=[CH:10][C:9]([O:17]C)=[CH:8][CH:7]=3)[CH2:3][CH2:2]1.B(Br)(Br)Br.C(Cl)Cl.O.C(OCC)(=O)C>C(Cl)Cl>[CH:1]1([C:4]2[N:5]([CH2:19][C:20]3[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=3)[C:6]3[C:11]([C:12]=2[CH2:13][C:14]([NH2:16])=[O:15])=[CH:10][C:9]([OH:17])=[CH:8][CH:7]=3)[CH2:2][CH2:3]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 962聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯]HCID 8857乙酸乙酯HCID 105928422-cyclopropyl-5-methoxy-1-(phenylmethyl)-1H-indole-3-acetamideHCID 22277759Boron tribromide dichloromethane

产物 1

HCID 106635022-cyclopropyl-5-hydroxy-1-(phenylmethyl)-1H-indole-3-acetamide收率 79%

试剂、催化剂与溶剂 1

HCID 6344
二氯甲烷
溶剂

实验过程

A solution of 400 mg (1.2 mmol) of 2-cyclopropyl-5-methoxy-1-(phenylmethyl)-1H-indole-3-acetamide and 2 mL of 1M BBr3/methylene chloride in 130 mL of methylene chloride was stirred for 1 hour with an ice-water bath and 3 hours at room temperature. The mixture was poured into water, 200 mL of ethyl acetate added, the organic layer separated, washed with brine and dried (Na2SO4). After concentrating at reduced pressure, the residue was crystallized from ethyl acetate to give 300 mg (79% yield) of 2-cyclopropyl-5-hydroxy-1-(phenylmethyl)-1H-indole-3-acetamide, mp, 174-175° C.

后处理

  1. additionadded
  2. customthe organic layer separated
  3. washwashed with brine
  4. dry with materialdried (Na2SO4)
  5. concentrationAfter concentrating at reduced pressure
  6. customthe residue was crystallized from ethyl acetate

来源与证据

ORD记录
ord-873fa58df45f427ab298a36f17bbb1d8
来源数据集
uspto-grants-2001_06
DOI
10.6084/m9.figshare.5104873.v1
专利号
US06252084B1

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