Reaktion #2055477

ord-b24ffc52afa3451a8935945cb157b228

Reaktionsgleichung

CCC(Cc1ccccc1)(C(=O)c1ccc(N2CCOCC2)cc1)N(C)C
Irgacure 369
O=C(c1ccccc1)C1(O)CCCCC1
Irgacure 184
O=C(OCCOCCOC(=O)C(=O)c1ccccc1)C(=O)c1ccccc1
Irgacure 754
CSc1ccc(C(=O)C(C)(C)N2CCOCC2)cc1
Irgacure 907
→
CC(C)c1ccc2sc3ccccc3c(=O)c2c1
Speedcure ITX
CCOC(=O)c1ccc(N(C)C)cc1
Speedcure EDB

Edukte

CCC(Cc1ccccc1)(C(=O)c1ccc(N2CCOCC2)cc1)N(C)C
Irgacure 369
O=C(c1ccccc1)C1(O)CCCCC1
Irgacure 184
O=C(OCCOCCOC(=O)C(=O)c1ccccc1)C(=O)c1ccccc1
Irgacure 754
CSc1ccc(C(=O)C(C)(C)N2CCOCC2)cc1
Irgacure 907

Reagenzien

Keine

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeproduced by Ciba Specialty Chemicals K

Vorschrift

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. An amount of the photopolymerization initiator to be added is preferably 0.1 to 10 parts by weight with respect to 100 parts by weight of the ionizing radiation-curable resin.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08422133B2uspto-grants-2013_04