반응식
[F:1][C:2]([F:11])([F:10])[C:3]1[S:4][CH:5]=[C:6]([CH2:8]O)[N:7]=1.S(Cl)(Cl)=O.[CH3:16][S-:17].[Na+].O>C(Cl)(Cl)Cl>[F:1][C:2]([F:11])([F:10])[C:3]1[S:4][CH:5]=[C:6]([CH2:8][S:17][CH3:16])[N:7]=1참가 물질
반응 조건
- 온도
- 25 °C
실험 절차
2-(Trifluoromethyl)4-thiazolemethanol (EP 402246; 1.5 g, 8.3 mmol) was dissolved in 15 ml chloroform, treated with thionyl chloride(1.8 ml, 2.4 g, 21 mmol) and heated to reflux. After 1h, the mixture was cooled and volatiles were removed under vacuum. The residue was taken up in 25 ml ethyl acetate and washed with 10 ml sat. NaHCO3, 10 ml sat. NaCl, dried(Na2SO4) and evaporated. The residue was taken up in 5 ml ethanol and treated in portions with sodium thiomethoxide (800 mg, 12 mmol) and stirred for 1 h at 25° C. The mixture was poured into 15 ml water and extracted 2× 15 ml ethyl acetate. The combined extracts were washed with sat. NaCl, dried(Na2SO4) and evaporated to obtain 1.3 g of 2-(Trifluoro-methyl)-4(methylthio)methyl thiazole (A).
후처리
- temperatureheated to reflux
- customvolatiles were removed under vacuum
- washwashed with 10 ml sat. NaHCO3, 10 ml sat. NaCl, dried(Na2SO4)
- customevaporated
- extractionextracted 2× 15 ml ethyl acetate
- washThe combined extracts were washed with sat. NaCl, dried(Na2SO4)
- customevaporated
출처 및 근거
- ORD 기록
- ord-cd44fa74dab247e485c19181a521991f
- 출처 데이터셋
- uspto-grants-2011_01
- 특허 번호
- US07863303B2
연결된 노트
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