HRID416063

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID7498

alpha-Bromotoluene

C7H7Br

HCID24758

Sodium hydride

HNa

结构：CC(C)(Oc1ccc(CCC(O)c2ccc(-c3ccc(C(F)(F)F)cc3)s2)c(Cl)c1Cl)C(=O)O

HCID25062866

未命名化合物

PRODUCTS

生成物

结构：CC(C)(Oc1ccc(CCC(OCc2ccccc2)c2ccc(-c3ccc(C(F)(F)F)cc3)s2)c(Cl)c1Cl)C(=O)O

HCID25059219

未命名化合物

PROCEDURE

实验过程

2-(4-(3-(Benzyloxy)-3-(5-(4-(trifluoromethyl)phenyl)thien-2-yl)propyl)-2,3-di-chlorophenoxy)-2-methylpropanoic acid is prepared from 2-(2,3-dichloro-4-(3-hydroxy-3-(5-(4-(trifluoromethyl)phenyl)thien-2-yl)propyl)phenoxy)-2-methylpropanoic acid using 2.2 equivalents of sodium hydride and 2.2 equivalents of benzyl bromide according to general procedure H.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-d06ccc499bd241ddb26635d3101de897
来源数据集: uspto-grants-2012_01
DOI: 10.6084/m9.figshare.5104873.v1
专利: US08088819B2
来源说明: uspto-grants-2012_01

反应 SMILES

[Cl:1][C:2]1[C:14]([Cl:15])=[C:13]([CH2:16][CH2:17][CH:18]([OH:34])[C:19]2[S:20][C:21]([C:24]3[CH:29]=[CH:28][C:27]([C:30]([F:33])([F:32])[F:31])=[CH:26][CH:25]=3)=[CH:22][CH:23]=2)[CH:12]=[CH:11][C:3]=1[O:4][C:5]([CH3:10])([CH3:9])[C:6]([OH:8])=[O:7].[H-].[Na+].[CH2:37](Br)[C:38]1[CH:43]=[CH:42][CH:41]=[CH:40][CH:39]=1>>[CH2:37]([O:34][CH:18]([C:19]1[S:20][C:21]([C:24]2[CH:25]=[CH:26][C:27]([C:30]([F:31])([F:32])[F:33])=[CH:28][CH:29]=2)=[CH:22][CH:23]=1)[CH2:17][CH2:16][C:13]1[CH:12]=[CH:11][C:3]([O:4][C:5]([CH3:9])([CH3:10])[C:6]([OH:8])=[O:7])=[C:2]([Cl:1])[C:14]=1[Cl:15])[C:38]1[CH:43]=[CH:42][CH:41]=[CH:40][CH:39]=1