Acetic Anhydride → 1-Acetoxy-1-methyl-silacyclobutane

HRID 1089316

反応式

HRID 1089316 の反応式
Cl[Si]1(Cl)CCC1.Cl[Si:8]1([CH3:12])[CH2:11][CH2:10][CH2:9]1.[C:13]([O:16]C(=O)C)(=[O:15])[CH3:14]>CO>[C:13]([O:16][Si:8]1([CH3:12])[CH2:11][CH2:10][CH2:9]1)(=[O:15])[CH3:14]

参加物

5

反応物 3

HCID 7918Acetic AnhydrideHCID 753731,1-DichlorosilacyclobutaneHCID 137554Silacyclobutane, 1-chloro-1-methyl-

生成物 1

HCID 198225581-Acetoxy-1-methyl-silacyclobutane

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

Several silacyclobutane monomers are known. For example, see U.S. Pat. No. 3,046,291 to Leo H. Sommer, and U.S. Pat. No. 3,687,995 to David Jonas et al. Sommer prepared his silacyclobutanes by reacting ClCH2CHRCH2SiR'Cl2 with magnesium. Jonas et al. teach organosilicon compounds having the general formula ##STR4## where R represents an atom or radical selected from the group consisting of hydrogen atom and alkyl radicals having less than 7 carbon atoms and R' represents alkoxy radicals having less than 5 carbon atoms or a radical of the formula -NR"2, in which each R" is a hydrogen atom .COPYRGT.r an alkyl radical. In U.S. Pat. No. 3,694,427, issued Sept. 26, 1972, Jonas et al. teach that R' can also be acyloxy radical. As an example, the reaction of 1,1-dichlorosilacyclobutane with methylorthoformate gave 1,1-dimethoxysilacyclobutane ##STR5## in 78% yield Further, the same compound was prepared in only 59% yield by reaction of 1,1-dichlorosilacyclobutane and methanol (Bush, R. Ph.D. Thesis, Univ. of California at Davis, 1975; Diss. Abstr. Int. B 1976, 36, 5034). Similarly, the reaction of 1-chloro-1-methyl-silacyclobutane and acetic anhydride gave 1-acetoxy-1-methyl-silacyclobutane ##STR6## in 48% yield (Nametkin, N. S.; Vdovin, V. M.; Grinberg, P. L. Dokl. Akad. Nauk SSSR. 1964, 155, 849 [320]) Silacyclobutane silazanes have been prepared by metathesis reaction with formation of alkali metal salt or condensation reaction with formation of HCl (Nametkin, N. S.; Vdovin, V. M.; Babich, E. D.; Oppengeim, V. D. Khim. Geterotsikl. Soedin., 1965 455) and British Patent No. 1,328,514 to Bush et al. These reactions generally give less than quantitative yields and require additional processing steps in comparison to the invention process. The invention process also provides novel compounds. See also Nametkin, N.S.; Vdovin, J. M.; Babich, E. D. Khim. Geterotsikl. Soedin., 1967, 148. Transsilylation of silazanes is taught and transsilylation of 1-chloro-1-methylsilacyclobutane with disilazanes is shown.

出典と根拠

ORDレコード
ord-7ed112c6c0f44a45810038ff5d83e3b1
出典データセット
uspto-grants-1990_10
特許番号
US04965367

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