Lithium Hydroxide → Benzyl 2-aminoethyl(methyl)carbamate
반응식
[CH2:1]([O:8][C:9](=[O:21])[N:10]([CH3:20])[CH2:11][CH2:12][NH:13]C(=O)C(F)(F)F)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Li+].[OH-]>CO.O>[CH2:1]([O:8][C:9](=[O:21])[N:10]([CH2:11][CH2:12][NH2:13])[CH3:20])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1참가 물질
5
실험 절차
To a solution of compound B (103.0 g, 340.7 mmol) in MeOH (1200 ml) was added a solution of LiOH (16.4 g, 681.4 mmol) in water (120 ml). The reaction mixture was stirred at room temperature for 3 h. Solvents were evaporated to ¾ of initial volume followed by dilution with water (400 ml). Solution was extracted with EtOAc (2×300 ml). The organic layer was washed with brine (200 ml), dried over MgSO4 and evaporated in vacuo. The resultant residue was dissolved in ether (300 ml) and treated with 2 N HCl/ether (200 ml). The formed precipitate was filtered, washed with ether and dried in vacuo to provide hydrochloric salt of compound C (54.5 g, 261.2 mmol) as white solid. LC-MS [M+H] 209.5 (C11H16N2O2+H, calc: 209.3).
후처리
- customSolvents were evaporated
- extractionSolution was extracted with EtOAc (2×300 ml)
- washThe organic layer was washed with brine (200 ml)
- dry with materialdried over MgSO4
- customevaporated in vacuo
- dissolutionThe resultant residue was dissolved in ether (300 ml)
- additiontreated with 2 N HCl/ether (200 ml)
- filtrationThe formed precipitate was filtered
- washwashed with ether
- customdried in vacuo
출처 및 근거
- ORD 기록
- ord-02f6731994344348a520b575b0b8c15a
- 출처 데이터셋
- uspto-grants-2014_08
- 특허 번호
- US08802681B2
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