참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Glycol monoethyl ether | HCID 8076 | — |
| 반응물 | Sodium Sulfide | HCID 14804 | — |
| 반응물 | Sodium | HCID 5360545 | — |
| 반응물 | 2,4-Diiminothiazolidinium benzenesulfonate | HCID 86734211 | — |
| 반응물 | HCID 178492520 | HCID 178492520 | — |
| 생성물 | HCID 178492518 | HCID 178492518 | — |
반응 단계
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 and the mixture stirred at 25° C. for a period of 1 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 was 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).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04122261 |
|---|
| 출처 데이터셋 | uspto-grants-1978_10 |
|---|
| ORD ID | ord-142447a1941f4ab294d3a64ef7116e27 |
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| 출처 메모 | uspto-grants-1978_10 |
|---|