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ChemicalBook CAS DataBase List 2-Benzylamino-2-methyl-1-propanol

2-Benzylamino-2-methyl-1-propanol synthesis

11synthesis methods
To a solution of 2-amino-2-methylpropan-1-ol (1 g, 11.22 mmol) and benzaldehyde (1.310 g, 12.34 mmol) in DCE (15 mL) at RT was added portionwise sodium triacetoxyborohydride (6.66 g, 31.4 mmol), and the mixture was stirred for 3 h. The mixture was diluted with EtOAc and washed with saturated aqueous NaHCO3. The organic layer was dried over MgSO4, filtered, and concentrated. The crude product 2-Benzylamino-2-methyl-1-propanol (1.247 g, 6.96 mmol, 62 % yield) was used without further purification. LCMS (m/z): 180.0 (M+H+).synthesis of 2-Benzylamino-2-methyl-1-propanol
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Yield:10250-27-8 96%

Reaction Conditions:

Stage #1:benzaldehyde;2-Amino-2-methyl-1-propanol in dichloromethane at 20; for 3 h;Molecular sieve;
Stage #2: with methanol;sodium tetrahydroborate at 20; for 1 h;

Steps:

9.a (a) 2-(Benzylamino)-2-methylpropan-1-ol
Benzaldehyde (3.4 mL, 33.7 mmol) was added dropwise to a stirred mixture of 2-amino- 2-methylpropan-1-ol (3.0 g, 33.7 mmol), 5 A molecular sieves (5 g) and CH2CI2(30 mL) at rt. The mixture was stirred at rt for 3 h, filtered through a pad of cotton and concentrated. MeOH (20 mL) followed by NaBH4(1.5 g, 40.4 mmol) was added and the mixture was stirred at rt for 1 h. NH4CI (aq, sat, 10 mL) was added and the mixture was concentrated, treated with NaOH (1 M, 20 mL) and extracted with EtOAc. The combined extracts were dried (Na2SO4) and concentrated to give the sub-title compound (5.8 g, 33.3 mmol, 96 %), which was used in the next step without further purification.

References:

ATROGI AB;PELCMAN, Benjamin;BENGTSSON, Tore WO2020/188299, 2020, A1 Location in patent:Page/Page column 59; 60

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