Sodium Acetate → HCID 14452902, 화합물
반응식
[NH2:1][C:2]1[C:3]([Cl:11])=[N:4][C:5]([CH2:9][CH3:10])=[CH:6][C:7]=1[Cl:8].[C:12]([O-])(=[O:14])[CH3:13].[Na+]>C(OC(=O)C)(=O)C>[C:12]([NH:1][C:2]1[C:3]([Cl:11])=[N:4][C:5]([CH2:9][CH3:10])=[CH:6][C:7]=1[Cl:8])(=[O:14])[CH3:13]참가 물질
실험 절차
7.8 g (40.8 mmol) of 3-amino-2,4-dichloro-6-ethyl-pyridine are heated under reflux for two hours in a mixture of 40 ml of acetic anhydride and 4 g (49 mmol) of anhydrous sodium acetate. The mixture is subsequently evaporated in vacuo, the residue is partitioned between dilute NH3 solution and CHCl3, and the organic phase is separated off, dried using Na2SO4 and evaporated. The residue (11.2 g) consists of a mixture of mono- and diacetylated amine. It is dissolved in 50 ml of methanol, 10 g of powdered K2CO3 are added and the mixture is stirred for one hour at room temperature. It is subsequently evaporated and partitioned between water and CHCl3, and the organic phase is separated off and washed with 5% strength aqueous NaH2PO4 solution. After drying using Na2SO4, the organic phase is evaporated. The residue is stirred with ether and filtered off with suction. Yield 7.7 g (80.9% of theory) melting point: 142° C.
후처리
- customThe mixture is subsequently evaporated in vacuo
- customthe residue is partitioned between dilute NH3 solution and CHCl3
- customthe organic phase is separated off
- customdried
- customevaporated
- additionThe residue (11.2 g) consists of a mixture of mono- and diacetylated amine
- dissolutionIt is dissolved in 50 ml of methanol
- addition10 g of powdered K2CO3 are added
- customIt is subsequently evaporated
- custompartitioned between water and CHCl3
- customthe organic phase is separated off
- washwashed with 5% strength aqueous NaH2PO4 solution
- customAfter drying
- customthe organic phase is evaporated
- stirringThe residue is stirred with ether
- filtrationfiltered off with suction
출처 및 근거
- ORD 기록
- ord-15bc2417e70f4dca9ca997e23f114d65
- 출처 데이터셋
- uspto-grants-1990_07
- 특허 번호
- US04939262
반응 노트
불러오는 중…