Ethyl orthoformate → Ethyl 1,2,4-oxadiazole-3-carboxylate
반응식
[OH:1][NH:2][C:3](=[NH:9])[C:4]([O:6][CH2:7][CH3:8])=[O:5].[CH2:10](OC(OCC)OCC)C>B(F)(F)F.CCOCC>[O:1]1[CH:10]=[N:9][C:3]([C:4]([O:6][CH2:7][CH3:8])=[O:5])=[N:2]1참가 물질
4
실험 절차
To a suspension of ethyl 2-(hydroxyamino)-2-iminoacetate (3 g, 22.71 mmol) in triethylorthoformate (14 mL, 84.08 mmol) was added boron trifluoride diethyl etherate (0.144 mL, 1.14 mmol). It was heated for 90 minutes. The reaction mixture was concentrated under reduced pressure and the residue dissolved in chloroform. The resulting organic layer was washed with aqueous hydrochloric acid 2N (2×80 mL), aqueous sodium bicarbonate 4% (1×80 mL) and water (2×80 mL), it was dried over anhydrous sodium sulphate and the solvent removed under reduced pressure to yield the title compound (2.70 g, 79%) as a yellow oil.
후처리
- temperatureIt was heated for 90 minutes
- concentrationThe reaction mixture was concentrated under reduced pressure
- dissolutionthe residue dissolved in chloroform
- washThe resulting organic layer was washed with aqueous hydrochloric acid 2N (2×80 mL), aqueous sodium bicarbonate 4% (1×80 mL) and water (2×80 mL), it
- dry with materialwas dried over anhydrous sodium sulphate
- customthe solvent removed under reduced pressure
출처 및 근거
- ORD 기록
- ord-bd97b84e6d7045a19546339bbf3e0cd5
- 출처 데이터셋
- uspto-grants-2012_09
- 특허 번호
- US08258122B2
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