HRID1968296

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID70355

(1-Hydroxycyclohexyl)(phenyl)methanone

C13H16O2

结构：CCC(Cc1ccccc1)(C(=O)c1ccc(N2CCOCC2)cc1)N(C)C

HCID86171

2-Benzyl-2-(dimethylamino)-1-[4-(morpholin-4-yl)phenyl]butan-1-one

C23H30N2O2

HCID92387

2-Methyl-4'-(methylthio)-2-morpholinopropiophenone

C15H21NO2S

结构：O=C(OCCOCCOC(=O)C(=O)c1ccccc1)C(=O)c1ccccc1

HCID60004985

Benzeneacetic acid, alpha-oxo-, 1,1'-(oxydi-2,1-ethanediyl) ester

C20H18O7

PRODUCTS

生成物

HCID25127

Parbenate

C11H15NO2

HCID79633

2-Isopropylthioxanthone

C16H14OS

PROCEDURE

实验过程

Specific examples include such as Irgacure 184, Irgacure 907, Irgacure 369, Irgacure 379, Irgacure 819, Irgacure 127, Irgacure 500, Irgacure 754, Irgacure 250, Irgacure 1800, Irgacure 1870, Irgacure OXE01, DAROCUR TPO and DAROCUR 1173, produced by Ciba Specialty Chemicals K. K.; Speedcure MBB, Speedcure PBZ, Speedcure ITX, Speedcure CTX, Speedcure EDB, Esacure ONE, Esacure KIP150, and Esacure KTO46, produced by Nihon SiberHegner K. K.; and KAYACURE DETX-S, KAYACURE CTX, KAYACURE BMS and KAYACURE DMBI, produced by Nippon Kayaku Co., Ltd. Among them, Irgacure 369, Irgacure 127, Irgacure 907, Esacure ONE, Speedcure MBB, Speedcure PBZ, and KAYACURE DETX-S are preferable.

WORKUP

后处理

customproduced by Ciba Specialty Chemicals K

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-da237bb321ab45088ebf297bc7047fbe
来源数据集: uspto-grants-2013_04
DOI: 10.6084/m9.figshare.5104873.v1
专利: US08422133B2
来源说明: uspto-grants-2013_04

反应 SMILES

[CH2:1]1[CH2:6][CH2:5][C:4](O)([C:7]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)=[O:8])[CH2:3][CH2:2]1.C[C:17](N1CCOCC1)([C:19](C1C=CC([S:27]C)=CC=1)=[O:20])C.[CH3:35][CH2:36][C:37](N(C)C)([C:45]([C:47]1[CH:52]=[CH:51][C:50]([N:53]2[CH2:58]COC[CH2:54]2)=[CH:49][CH:48]=1)=[O:46])CC1C=CC=CC=1.C1C=CC(C(C(OCCOCCOC(C(C2C=CC=CC=2)=O)=O)=O)=O)=CC=1>>[CH3:35][CH:36]([C:6]1[CH:1]=[CH:2][C:3]2[S:27][C:14]3[C:9]([C:7](=[O:8])[C:4]=2[CH:5]=1)=[CH:10][CH:11]=[CH:12][CH:13]=3)[CH3:37].[CH3:17][CH2:19][O:20][C:45]([C:47]1[CH:48]=[CH:49][C:50]([N:53]([CH3:54])[CH3:58])=[CH:51][CH:52]=1)=[O:46]