반응식
C[N:2]([CH3:4])Cl.[Cl-].[Al+3].[Cl-].[Cl-].C(OCC)C.[CH2:14]=[CH:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26]C.Cl>C(Cl)Cl.O>[CH2:4]([NH2:2])[CH2:26][CH2:25][CH2:24][CH2:23][CH2:22][CH2:21][CH2:20][CH2:19][CH2:18][CH2:17][CH2:16][CH2:15][CH3:14]참가 물질
반응 조건
- 온도
- -35 °C
실험 절차
To a reactor of the type used in Example 1 is charged a cold solution of N,N-dimethylchloramine (0.87 moles), chilled to -77° C, in 300 ml of methylene chloride, followed by aluminum chloride (0.3 moles). The mixture is stirred for 5 minutes and then diethyl ether (0.4 moles) is added. After stirring for an additional 5 minutes, an additional portion of diethyl ether (0.4 moles) and 1-tetradecene (0.3 mol) is added to the stirred solution. The chilled reaction mixture is heated to -35° C and the reaction mixture stirred for one hour. At the end of this time an 80 g portion of hydrochloric acid (28% by weight) and 100-300 g of water are added to the reaction mixture and stirred for a half hour. The organic and water layers are then separated and the organic layer is stirred for an additional half-hour with 80 g of the same strength hydrochloric acid used previously. Again the organic and water layers are separated. The organic layer is filtered to yield 0.02 mol of tetradecyl amine salt. This represents a 6.68% yield based on the amount of 1-tetradecene charged.
후처리
- customTo a reactor of the type used in Example 1
- stirringAfter stirring for an additional 5 minutes
- customThe chilled reaction mixture
- stirringthe reaction mixture stirred for one hour
- stirringstirred for a half hour
- customThe organic and water layers are then separated
- stirringthe organic layer is stirred for an additional half-hour with 80 g of the same strength hydrochloric acid
- customAgain the organic and water layers are separated
- filtrationThe organic layer is filtered
출처 및 근거
- ORD 기록
- ord-45cce49d3e3a414c9c9dd87baa548fdc
- 출처 데이터셋
- uspto-grants-1978_05
- 특허 번호
- US04089903
연결된 노트
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