HRID479651

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID10727680

未命名化合物

HCID18772259

未命名化合物

HCID59110703

未命名化合物

PRODUCTS

生成物

结构：CCCc1cc(Oc2ccc(CC(C)C)cc2)ccc1OCCCOc1ccc2c(c1)O[C@@](CCC)(C(=O)O)CC2

HCID10166486

未命名化合物

PROCEDURE

实验过程

The title compound was prepared following the procedures described in Example 17, Step B-C employing (2R)-methyl 2-propyl-7-hydroxychromane-2-carboxylate instead of ethyl 7-hydroxychromane-2-carboxylate, and 2-propyl-4-(4-isobutylphenoxy)phenol (U.S. Pat. No. 6,008,237) instead of 2-chloro-4-phenoxyphenol.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-44f1c4665bc144a29b272fa34a1973a8
来源数据集: uspto-grants-2003_11
DOI: 10.6084/m9.figshare.5104873.v1
专利: US06645997B2
来源说明: uspto-grants-2003_11

反应 SMILES

[CH2:1]([C@:4]1([C:15]([O:17]C)=[O:16])[CH2:13][CH2:12][C:11]2[C:6](=[CH:7][C:8]([OH:14])=[CH:9][CH:10]=2)[O:5]1)[CH2:2][CH3:3].[CH2:19]([C:22]1[CH:27]=[C:26]([O:28][C:29]2[CH:34]=[CH:33][C:32]([CH2:35][CH:36]([CH3:38])[CH3:37])=[CH:31][CH:30]=2)[CH:25]=[CH:24][C:23]=1[OH:39])[CH2:20][CH3:21].Cl[C:41]1[CH:46]=C(OC2C=CC=CC=2)C=C[C:42]=1O>>[CH2:19]([C:22]1[CH:27]=[C:26]([O:28][C:29]2[CH:30]=[CH:31][C:32]([CH2:35][CH:36]([CH3:38])[CH3:37])=[CH:33][CH:34]=2)[CH:25]=[CH:24][C:23]=1[O:39][CH2:42][CH2:41][CH2:46][O:14][C:8]1[CH:7]=[C:6]2[C:11]([CH2:12][CH2:13][C@:4]([CH2:1][CH2:2][CH3:3])([C:15]([OH:17])=[O:16])[O:5]2)=[CH:10][CH:9]=1)[CH2:20][CH3:21]