참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2-Thiopheneacetic acid | HCID 15970 | — |
| 반응물 | Formicin | HCID 69365 | — |
| 용매 | Trifluoroacetic acid | HCID 6422 | — |
| 생성물 | 2-[5-(Acetamidomethyl)thiophen-2-yl]acetic acid | HCID 23330367 | — |
반응 단계
1.42 g of 2-thienylacetic acid are added in portions to a solution, kept at 0°-5° C., of 1.34 g of N-hydroxymethyl acetamide (Einhorn, Ann. Chem., volume 343, page 264 (1905)) in 10 ml of trifluoroacetic acid, whilst stirring. The mixture is stirred for 2 hours at 0°-5° C. and the trifluoroacetic acid is distilled off under reduced pressure. 30 ml of water are added to the residue and the mixture is extracted with twice 50 ml of ethyl acetate. The organic extracts are washed with a saturated aqueous sodium chloride solution, dried over magnesium sulphate, concentrated under reduced pressure and filtered through silica gel. The residue is crystallised from ethyl acetate and gives 2-(5-acetylaminomethyl-2-thienyl)-acetic acid, thin layer chromatogram (silica gel): Rf=0.61 (system: butanol/acetic acid/water, 45:45:10); infrared absorption spectrum (mineral oil): characteristic bands at 2.95μ, 5.82μ, 6.23μ and 6.38μ.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04234578 |
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| 출처 데이터셋 | uspto-grants-1980_11 |
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| ORD ID | ord-7ab72f441ead46f0a1bceb54cbcbabec |
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| 출처 메모 | uspto-grants-1980_11 |
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