참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Thiophene-3-carboxylic acid | HCID 6918 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Isobutyl chloroformate | HCID 62365 | — |
| 반응물 | 4-Ethyl-2-propyl semicarbazide | HCID 19010929 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 4-Ethyl-2-propyl-1-(3-thenoyl) semicarbazide | HCID 54099638 | — |
반응 단계
A stirred solution of 2.62 g (20.5 mmol) of thiophene-3-carboxylic acid and 2.8 mL (20.0 mmol) of triethylamine in 20 mL of THF was cooled to 5° C. and 2.6 mL (20.0 mmol) of isobutyl chloroformate was added dropwise over 5 minutes. The mixture was stirred at 5° C. for 5 minutes and added to a suspension of the 4-ethyl-2-propyl semicarbazide prepared above in 20 mL of THF at 5° C. This mixture was allowed to warm to room temperature and stirred overnight. The mixture was concentrated to remove most of the solvent, taken up in 75 mL of water and extracted with two 100 mL portions of ethyl acetate. The combined ethyl acetate extracts were washed with 50 mL of 5% aqueous HCl and 50 mL of saturated aqueous sodium bicarbonate (NaHCO3), and dried over MgSO4. Removal of the solvent left 5.30 g of crude 4 -ethyl-2-propyl-1-(3-thenoyl) semicarbazide as an oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05334726 |
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| 출처 데이터셋 | uspto-grants-1994_08 |
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| ORD ID | ord-3788da22400547588000d5e5ed67015c |
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| 출처 메모 | uspto-grants-1994_08 |
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