참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Benzocaine | HCID 2337 | — |
| 반응물 | Hydrazine | HCID 9321 | — |
| 반응물 | Thiophosgene | HCID 10040 | — |
| 반응물 | Ethyl 4-isothiocyanatobenzoate | HCID 71003 | — |
| 반응물 | 4-Ethoxycarbonylphenylthiosemicarbazide | HCID 19745752 | — |
| 반응물 | Sodium Nitrite | HCID 23668193 | — |
| 용매 | Ethanol | HCID 702 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Chloroform | HCID 6212 | — |
| 생성물 | HCID 178468779 | HCID 178468779 | 90% |
반응 단계
0.1 Mol of ethyl p-aminobenzoate was mixed with 150 ml of water and stirred for 15 minutes. Thiophosgene (10 g) in 50 ml chloroform was added dropwise. The mixture was stirred for 2 hours at 15° C. The organic solution was washed with HCl 2N, dried and the solvent was removed under vacuum to obtain a yellow-red oil, that was used as crude product. 0.02 mMole of the obtained 4-ethoxycarbonylphenylisothiocyanate and 30 ml ethanol were stirred in a flask and added dropwise with 2 ml 85% hydrazine in 2 ml water. After 15 minutes the crude product separated and was filtered under vacuum. Yield 90%. 0.01 Mole of the obtained 4-ethoxycarbonylphenylthiosemicarbazide was mixed with a solution of 1.5 ml HCl 37% and 35 ml water. The mixture was cooled to 5° C. and 0.8 g sodium nitrite dissolved in 5 ml water was added dropwise. The mixture was stirred for 30 minutes at 5° C. The crude product was filtered, washed with water and dried. Yield 80%. The product was crystallized from methanol. The structure was confirmed by IR and NMR spectroscopy.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05232826 |
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| 출처 데이터셋 | uspto-grants-1993_08 |
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| ORD ID | ord-6bb0f49f7b484b7d9fc48c25f6532664 |
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| 출처 메모 | uspto-grants-1993_08 |
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