Ammonia → 1-Amino-3-({[4-(aminomethyl)cyclohexyl]methyl}amino)propan-2-ol
반응식
[CH:1]1([CH2:9][NH2:10])[CH2:6][CH2:5][CH:4]([CH2:7][NH2:8])[CH2:3][CH2:2]1.[CH2:11]([CH:13]1[O:15][CH2:14]1)Cl.[OH-].[NH4+:17].C(Cl)C(O)C.N>CO>[NH2:17][CH2:11][CH:13]([OH:15])[CH2:14][NH:8][CH2:7][CH:4]1[CH2:5][CH2:6][CH:1]([CH2:9][NH2:10])[CH2:2][CH2:3]1참가 물질
반응 조건
- 온도
- 20 °C
실험 절차
1,4-Cyclohexanebis(methylamine) (14.2 g., 0.1 mole) is dissolved in 50 ml. of anhydrous methyl alcohol and the solution cooled to +5° C. in an ice bath. Epichlorohydrin (9.3 g., 0.1 mole) is added in a 2-minute period and the temperature maintained at +5° C. for 2 hours; reaction is allowed to continue at 10°-15° C. until thin layer chromatography of an aliquot (silica gel plate with development using a solution of 1 volume concentrated aqueous ammonium hydroxide in 4 volumes of methyl alcohol) indicated nearly complete conversion of the starting diamine to the propylene chlorohydrin. The solution is then added to 100 ml. of dry methyl alcohol previously saturated at 0° C. with dry ammonia gas by continuous dropwise flow at +5° C. with good agitation and external cooling. After stirring 2 hours at +5° C., it is allowed to warm to 20° C. and mixed overnight. The reaction is competed by heating at 45°-55° C. for 6 hours. The solvent and ammonia was removed by stripping and the product purified using fractional distillation under reduced pressure.
후처리
- temperaturethe temperature maintained at +5° C. for 2 hours
- customreaction
- customto continue at 10°-15° C. until thin layer chromatography of an aliquot
- additionThe solution is then added to 100 ml
- custompreviously saturated at 0° C.
- customat +5° C.
- additionmixed overnight
- temperatureby heating at 45°-55° C. for 6 hours
- customThe solvent and ammonia was removed
- customthe product purified
- distillationdistillation under reduced pressure
출처 및 근거
- ORD 기록
- ord-c6ea3f60e7444979a4763b1e39a658b2
- 출처 데이터셋
- uspto-grants-1977_09
- 특허 번호
- US04049417
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