2,3-Dihydro-7-nitrobenzofuran → 2,3-Dihydro-1-benzofuran-7-amine
반응식
[N+:1]([C:4]1[C:12]2[O:11][CH2:10][CH2:9][C:8]=2[CH:7]=[CH:6][CH:5]=1)([O-])=O.[H][H]>O1CCCC1.[Ni]>[O:11]1[C:12]2[C:4]([NH2:1])=[CH:5][CH:6]=[CH:7][C:8]=2[CH2:9][CH2:10]1참가 물질
5
실험 절차
39.4 g of 2,3-dihydro-7-nitrobenzofuran (prepared by the method described in Journal of Heterocyclic Chemistry, vol. 5, No. 1, p. 1 (1968)) in 200 ml of tetrahydrofuran was hydrogenated in a Parr shaker (50 p.s.i.g. hydrogen pressure, Raney nickel catalyst, 3 hours, room temperature). The resulting mixture was filtered and the solvent was evaporated from the filtrate. The residue was recrystallized from ether to give 1, as a colorless solid, m.p.: 70°-72° C.
후처리
- filtrationThe resulting mixture was filtered
- customthe solvent was evaporated from the filtrate
- customThe residue was recrystallized from ether
- customto give 1
출처 및 근거
- ORD 기록
- ord-a79c8dbe5eca475eb041554c08765875
- 출처 데이터셋
- uspto-grants-1981_11
- 특허 번호
- US04302592
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