Ethyl formate → 2-(N-Formylaminomethyl)benzoxazole
반응식
[NH2:1][CH2:2][C:3]1[O:4][C:5]2[CH:11]=[CH:10][CH:9]=[CH:8][C:6]=2[N:7]=1.[CH:12](OCC)=[O:13]>>[CH:12]([NH:1][CH2:2][C:3]1[O:4][C:5]2[CH:11]=[CH:10][CH:9]=[CH:8][C:6]=2[N:7]=1)=[O:13]참가 물질
3
실험 절차
A mixture of 4.29 g (28.9 mmol) of 2-(aminomethyl)benzoxazole (PREPARATION 6) and 20 ml of ethyl formate is heated at 80° for 2 hr, after which the excess ethyl formate is removed under reduced pressure. The residue is chromatographed on silica gel (350 ml) eluting with methanol/dichloromethane (2/98), the appropriate fractions are pooled and concentrated to give the product, which is crystallized from dichloromethane/hexane to give the title compound, mp 98°-99°; MS (m/z) at 176; IR 1655, 1621, 1519, 1241, 750 cm-1 ; NMR (CDCl3) 4.81, 6.45, 7.36, 7.53, 7.70, 8.39 δ.
후처리
- temperatureis heated at 80° for 2 hr
- customafter which the excess ethyl formate is removed under reduced pressure
- customThe residue is chromatographed on silica gel (350 ml)
- washeluting with methanol/dichloromethane (2/98)
- concentrationconcentrated
- customto give the product, which
- customis crystallized from dichloromethane/hexane
출처 및 근거
- ORD 기록
- ord-660bb5f6e5874854ba03701b091a1278
- 출처 데이터셋
- uspto-grants-1997_09
- 특허 번호
- US05668282
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