Triethylamine → HCID 71239712, 화합물
반응식
[CH2:1]([O:8][CH:9]1[CH2:14][CH2:13][CH:12]([C:15]([OH:17])=O)[CH2:11][CH2:10]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C([N:20](CC)CC)C.ClC(OCC)=O>C(Cl)Cl>[CH2:1]([O:8][CH:9]1[CH2:14][CH2:13][CH:12]([C:15]([NH2:20])=[O:17])[CH2:11][CH2:10]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1참가 물질
반응 조건
- 온도
- -15 °C
실험 절차
To a solution of 4-(benzyloxy)cyclohexanecarboxylic acid (5.4 g, 23 mmol, 1.0 equiv) and triethylamine (4.82 mL, 34.57 mmol, 1.5 equiv) in DCM (dry, 40 mL) was added ethyl chloroformate (3.0 mL, 31.1 mmol, 1.35 equiv) dropwise between −20 and −10° C. under N2. The white precipitate appeared. The mixture was stirred at about −15° C. for 10 min, dried NH3 was bubbled rapidly into the liquid for 20 min. The mixture was stirred at −15° C. for 30 min, then put into the fridge (−20° C.) overnight. The flask was released the pressure and warm to room temperature. H2O (100 mL) was added. The layer was separated and the aqueous phase was extracted with DCM (3×100 mL). The combined organic solution was washed with brine (50 mL), dried over anhydrous Na2SO4, concentrated to give 5.2 g (96.7%) of 4-(benzyloxy)cyclohexanecarboxamide as a off-white solid.
후처리
- customdried NH3 was bubbled rapidly into the liquid for 20 min
- stirringThe mixture was stirred at −15° C. for 30 min
- customput into the fridge (−20° C.) overnight
- temperaturewarm to room temperature
- additionH2O (100 mL) was added
- customThe layer was separated
- extractionthe aqueous phase was extracted with DCM (3×100 mL)
- washThe combined organic solution was washed with brine (50 mL)
- dry with materialdried over anhydrous Na2SO4
- concentrationconcentrated
출처 및 근거
- ORD 기록
- ord-bb5d09f9f3984a20b1bdf23031a2cc74
- 출처 데이터셋
- uspto-grants-2016_01
- 특허 번호
- US09226923B2
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