Organic compounds -- part of the class 532-570 series – Organic compounds – Oxygen containing
Reexamination Certificate
2003-12-18
2008-12-30
Shiao, Rei-tsang (Department: 1626)
Organic compounds -- part of the class 532-570 series
Organic compounds
Oxygen containing
Reexamination Certificate
active
07470824
ABSTRACT:
Provided is an adamantane derivative represented by Formula (I) or (II):wherein X represents a halogen atom; Y represents an alkyl group having 1 to 10 carbon atoms, a halogenated alkyl group having 1 to 10 carbon atoms, a halogen atom or a hetero atom-containing group; R1to R4represent independently hydrogen, a halogen atom, an alkyl group having 1 to 10 carbon atoms or a halogenated alkyl group having 1 to 10 carbon atoms; m represents an integer of 0 to 15, and n represents an integer of 0 to 10; and excluded is a case where in Formula (I), m and n are 0 at the same time and R3and R4are a hydrogen atom at the same time.Capable of being provided is a novel adamantane derivative which is useful as a modifying agent for a resin for a photoresist and a dry etching resistance-improving agent in the photolithography field, agricultural and medical intermediates and other various industrial products.
REFERENCES:
patent: 6440636 (2002-08-01), Ushirogouchi et al.
patent: 2002/0115883 (2002-08-01), Ogata et al.
patent: 119 008 (1901-03-01), None
patent: 02/36533 (2002-05-01), None
McMurry, John “Organic Chemistry—Fourth Edition” Brooks/Cole Publishing Company, 1996, pp. 816-818.
Okada et al. “Amino Acids and Peptides. L. Development of a Novel N-pi-Protecting Group for Histidine, N-pi-2-Adamantyloxymethylhistidine, and Its Application to Peptide Synthesis” Chem Pharm Bull, 1997, vol. 45, pp. 452-456.
Ben-David et al. “A novel synthesis of trifluoromethyl ethers via xanthates, utilizing BrF3” Journal of Fluorine Chemistry, 1999, vol. 97, pp. 75-78.
Machula, A. A. et al., “Radiochemical alkylation of adamantane by perfluorovinyl ethers”, Khimiya Vysokikh Energii, vol. 24, No. 2, pp. 117-121, 1990.
Database Crossfire Beilstein, Beilstein Institut zur Foerderung der Chemischen Wissenschaften, XP002367361, Palfray, Sabetay: Bull. Soc. Chim. Fr., <4> 43, p. 900, 1928.
Farren, J.W. et al., Chloro Ethers. II. Preparation of Some New Chloro Ethers and Alkoxymethyl Esters, J. AM. Chem. Soc., vol. 47, pp. 2419-2423, 1925.
Ben-David, Iris et al., “A novel synthesis of trifluoromethyl ethers via xanthates, utilizing BrF3”, Journal of Fluorine Chemistry, vol. 97, No. 1-2, pp. 75-78, 1999. 0009.
Okada, Yoshio et al., “Amino acids and peptides. L. Development of a Novel Nπ-protecting group for histidine, Nπ-adamantyloxymethylhistidine, and its application to peptide synthesis”, Chemical and Pharmaceutical Bulletin, vol. 45, No. 3, pp. 452 to 456, 1997.
Moss, Robert A. et al., “Absolute Kinetics of Alkoxychlorocarbene Fragmentation”, Journal of the American Chemical Society, vol. 118, No. 40, pp. 9792 to 9793, 1996.
Rykov, S.V. et al., Photochemical reactions of some mono- and diketo derivatives of adamantane in different solvents, Izvestiya Akademii Nauk, Seriya Kimicheskaya, No. 9, pp. 1833 to 1835. 0039.
Pericas, Miquel A. et al., Efficient synthesis of tert-alkoxy ethynes, Tetrahedron, vol. 43, No. 10, 2311 to 2316.
Hatakeyama Naoyoshi
Kodoi Kouichi
Ono Hidetoshi
Tanaka Shinji
Idemitsu Kosan Co. Ltd.
Kosack Joseph R
Oblon & Spivak, McClelland, Maier & Neustadt P.C.
Shiao Rei-tsang
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