HRID1792395

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：COCOc1ccc(C2(C)COc3cc(OCOC)ccc3C2CCCCCCCCCO[Si](C)(C)C(C)(C)C)cc1

HCID22033006

未命名化合物

结构：COCOc1ccc2c(c1)OCC(C)C2C#CCCCCCCCO[Si](C)(C)C(C)(C)C

HCID131725858

未命名化合物

PRODUCTS

生成物

结构：COCOc1ccc2c(c1)OCC(C)(c1ccc(O)cc1)C2CCCCCCCCCO[Si](C)(C)C(C)(C)C

HCID23537979

未命名化合物

PROCEDURE

实验过程

The title compound was prepared from 3-(4-benzyloxy]phenyl)-4-[9-(t-butyldimethylsilyloxy)-1-nonynyl]-7-methoxymethyloxy-3-methylchroman according to the same method for the synthesis of 4-[9-(t-butyldimethylsilyloxy)-1-nonyl]-7-methoxymethyloxy-3-(4-methoxymethyloxyphenyl)-3-methylchroman described in International Patent Appln. No. PCT/KR97/00265.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-28aa8e3571ed4446a2010d33b45c1a23
来源数据集: uspto-grants-2006_07
DOI: 10.6084/m9.figshare.5104873.v1
专利: US07074819B2
来源说明: uspto-grants-2006_07

反应 SMILES

[Si](OCCCCCCCC#CC1C2C(=CC(OCOC)=CC=2)OCC1C)(C(C)(C)C)(C)C.[Si:33]([O:40][CH2:41][CH2:42][CH2:43][CH2:44][CH2:45][CH2:46][CH2:47][CH2:48][CH2:49][CH:50]1[C:59]2[C:54](=[CH:55][C:56]([O:60][CH2:61][O:62][CH3:63])=[CH:57][CH:58]=2)[O:53][CH2:52][C:51]1([C:65]1[CH:70]=[CH:69][C:68]([O:71]COC)=[CH:67][CH:66]=1)[CH3:64])([C:36]([CH3:39])([CH3:38])[CH3:37])([CH3:35])[CH3:34]>>[Si:33]([O:40][CH2:41][CH2:42][CH2:43][CH2:44][CH2:45][CH2:46][CH2:47][CH2:48][CH2:49][CH:50]1[C:59]2[C:54](=[CH:55][C:56]([O:60][CH2:61][O:62][CH3:63])=[CH:57][CH:58]=2)[O:53][CH2:52][C:51]1([C:65]1[CH:66]=[CH:67][C:68]([OH:71])=[CH:69][CH:70]=1)[CH3:64])([C:36]([CH3:39])([CH3:37])[CH3:38])([CH3:35])[CH3:34]