HRID1591008

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：O=[N+]([O-])c1ccc(Oc2ccc(O)cc2)c(Cl)c1

HCID12940628

4-(2-Chloro-4-nitrophenoxy)phenol

C12H8ClNO4

结构：CC(Oc1ccc(Oc2ccc(C(F)(F)F)cn2)cc1)C(=O)Cl.Cl

HCID88451400

未命名化合物

PRODUCTS

生成物

结构：CC(Oc1ccc(Oc2ccc(C(F)(F)F)cn2)cc1)C(=O)Oc1ccc(Oc2ccc([N+](=O)[O-])cc2Cl)cc1

HCID14498585

未命名化合物

PROCEDURE

实验过程

In Example 1-13, by using 2-(4-(5-trifluoromethyl-2-pyridyloxy)phenoxy)propionic acid chloride hydrochloride instead of 2-(4-(3-chloro-5-trifluoromethyl-2-pyridyloxy)phenoxy)propionic acid chloride hydrochloride, and 4-(2-chloro-4-nitrophenoxy)phenol instead of 4-(4-nitrophenoxy)phenol, 4-(2-chloro-4-nitrophenoxy)phenyl 2-(4-(5-trifluoromethyl-2-pyridyloxy)phenoxy)propionate was obtained.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-64b4f7226b4d438a99913257db83341e
来源数据集: uspto-grants-1993_04
DOI: 10.6084/m9.figshare.5104873.v1
专利: US05205855
来源说明: uspto-grants-1993_04

反应 SMILES

Cl.[F:2][C:3]([F:24])([F:23])[C:4]1[CH:5]=[CH:6][C:7]([O:10][C:11]2[CH:22]=[CH:21][C:14]([O:15][CH:16]([CH3:20])[C:17](Cl)=[O:18])=[CH:13][CH:12]=2)=[N:8][CH:9]=1.[Cl:25][C:26]1[CH:39]=[C:38]([N+:40]([O-:42])=[O:41])[CH:37]=[CH:36][C:27]=1[O:28][C:29]1[CH:34]=[CH:33][C:32]([OH:35])=[CH:31][CH:30]=1>>[F:2][C:3]([F:24])([F:23])[C:4]1[CH:5]=[CH:6][C:7]([O:10][C:11]2[CH:22]=[CH:21][C:14]([O:15][CH:16]([CH3:20])[C:17]([O:35][C:32]3[CH:33]=[CH:34][C:29]([O:28][C:27]4[CH:36]=[CH:37][C:38]([N+:40]([O-:42])=[O:41])=[CH:39][C:26]=4[Cl:25])=[CH:30][CH:31]=3)=[O:18])=[CH:13][CH:12]=2)=[N:8][CH:9]=1