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HRID 1833517作成日:2026年10月25日

Glycol monoethyl ether → HCID 178492518、化合物

https://huagongshe.com/reaction/1833517

反応式

関与物質

役割名称HCID仕込み量
反応物Glycol monoethyl etherHCID 8076—
反応物Sodium SulfideHCID 14804—
反応物SodiumHCID 5360545—
反応物2,4-Diiminothiazolidinium benzenesulfonateHCID 86734211—
反応物HCID 178492520HCID 178492520—
生成物HCID 178492518HCID 178492518—

反応条件

温度25 °C

反応手順

To 140 parts of 2-ethoxyethanol stirred at 100° C under an atmosphere of nitrogen there was added 8.6 parts of 60 percent active solid sodium sulfide and the resultant solution was filtered to remove undissolved material. The filtrate was mixed with 94 parts of dimethylformamide and 11.3 parts of 3,6-dimethoxy-phthalonitrile nd the mixture stirred at 25° C for a period of one hour. The reaction mixture was then heated to 95° C over a period of 1 hour, cooled to 25° C and filtered to remove undissolved material which was found to be (4.5 parts) unreacted 3,6-dimethoxyphthalonitrile. The filtrate, which contained approximately 0.04 mole of the sodium salt of 4,7-dimethoxy-1-imino-3-mercaptoisoindoline was stirred and there as added 10.7 parts of 2,4-diiminothiazolidinium benzenesulfonate. Stirring was continued overnight at 25° C. The product which separated was collected by filtration, washed successively with four portions of 12.0 parts each of methyl alcohol and finally dried in vacuo to obtain 4.5 parts of 4,7-dimethoxy-1-imino-3-(2,4-diimino-5-thiazolidinylidene)isoindoline as a red solid which melted at 227°-246° C (dec).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04066653
出典データセットuspto-grants-1978_01
ORD IDord-b12d6b10e5404adbb1dc3e3afa4d2fcc
出典メモuspto-grants-1978_01