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ChemicalBook CAS DataBase List N-BOC-1,6-diaminohexane
51857-17-1

N-BOC-1,6-diaminohexane synthesis

12synthesis methods
synthesis of N-BOC-1,6-diaminohexane: 1,6-Diaminohexane 3 (Fig. 1) (100 g, 0.86 mol) was dissolved in CH2Cl2 (300 ml) and cooled in an ice bath to 0–3°C. To the stirred solution 0.3 eq. di-tert-butyl bicarbonate (62.6 g, 0.29 mol) was added slowly over a period of 1 h. The reaction was allowed to warm up to r.t., and proceeded overnight. The reaction mixture was extracted with saturated aqueous NaHCO3 (50 ml, three times). The organic phases were pooled, dried, and evaporated under reduced pressure. The resulting oil was dissolved in 200 ml, 1 N HCl and extracted with ether. The aqueous phase was washed with ether, made basic to a pH of 10 with aqueous 2 N NaO3, and extracted with ethyl acetate. The organic phases were pooled, dried, and evaporated under reduced pressure. The resulting oil was dissolved in 200 ml, 1 N HCL and extracted with ether. The aqueous phase was washed with ether, made basic to a pH of 10 with aqueous 2 N NaOH, and extracted with ethyl acetate. The organic extracts were pooled, dried over Na2SO4 and evaporated to give 10.5 g of homogeneous N-BOC-1, 6- diaminohexane 2c (Fig. 1) as a yellow oil which was used without further purification.
TLC Rf 0.51; 1H NMR (CDCL3) d 4.54 (bs, 1H; NH), 3.05 1 2.62 (m, 4H; NCH2), 1.41 (m, 9H; CH3), 1.29 (m, 8H; CH2).
Evaluation of aminoalkylmethacrylate nanoparticles as colloidal drug carrier systems. Part I: synthesis of monomers, dependence of the physical properties on the polymerization methods
129392-87-6 Synthesis
6-AZIDO-N-BOC-HEXYLAMINE

129392-87-6
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Yield:51857-17-1 97%

Reaction Conditions:

with hydrogen;palladium on activated charcoal at 20; under 3102.97 Torr; for 1 h;

Steps:

A [6-T-BUTYLOXYCARBAMOYLHEXYLAMINE] (4).
A solution of di-t-butyldicarbonate (18.6 g, [85.] 3 mmol) in dry DCM (100 [ML)] was added dropwise to a stirred solution of 6- aminohexanol (10.0 g, 85.3 mmol) in dry DCM (100 [ML)] at 20 [°C] and stirred for 16 h. The solution was washed with dilute aqueous [NA2C03] solution (100 mL), 0.1 M HC1 (100 mL), water (100 mL), brine (50 mL), dried and the solvent evaporated. The residue was dissolved in DCM (250 mL) and Et3N (15.5 mL, 111 mmol) added. A solution of methanesulfonyl chloride (7.3 mL, 94 mmol) was added dropwise and the mixture stirred at [20 °C] for 16 h. The solution was washed with saturated aqueous [KHC03] (100 mL), water (2 x 100 mL), brine (50 mL), dried, and the solvent evaporated. The residue was dissolved in DMF (100 [ML)] and NaN3 [(5.] 55 g, [85.] 3 mmol) added. The mixture was stirred at [100 °C] for 1 h, the solvent evaporated and the residue partitioned between EtOAc (200 mL) and water (200 mL). The organic fraction was washed with water (200 mL), brine (100 mL), dried and the solvent evaporated. The residue was purified by chromatography, eluting with 30% EtOAc/pet. ether, to give the [6-T-BUTYLOXYCARBAMOYLHEXYL] azide (17.5 g, 85%) as a colorless [OIL, 1H NMR 8] 4.53 (br s, 1 H, OCONH), 3.52 (t, J= 6.9 Hz, 2 H, [CH2N),] 3.11 (dt, [J=] 6.5, 6.4 Hz, 2 H, [CH2N),] 1.57-1. 63 (m, 2 H, [CH2),] 1.44-1. 52 (m, 11 H, CH2, C [(CH3)] 3), 1.30-1. 40 (m, 4 H, 2 x [CH2), 13C NMR 8] 156.0, 79.1, 51.3, 40.4, 29.9, 28.7, 28.4 (3), 26.4, 26.3. [A] mixture of azide (14.81 g, 61.1 mol) and Pd/C (0.5 g) in EtOAc/EtOH (200 mL) was stirred at [20 °C] under hydrogen (60 psi) for 1 h. The mixture was filtered through celite, the cake washed with EtOAc [(3 X 30] mL) and the solvent evaporated to give 4 (12.82 g, [97%)] as a white solid, mp (EtOAc) [89-91 °C] ; 1H NMR 8 4.65 (br s, 1 H, OCONH), 3.52 (br s, 2 H, NH2), 2.69 (t, [J=] 6.9 Hz, 2 H, CH2N), 1. 88 (br s, 2 H, CH2N), 1.44-1. 50 [m, 13 H, 2 x [CHA,] C (CH3) 3], 1.29-1. 35 (m, 4 H, 2 x [CHEZ) ; 13C] NMR 8 156.0, 78.9, 41.9, 40.4, 33.4, 29.9, 28.3 (3), 26.5, 26.4.

References:

AUCKLAND UNISERVICES LIMITED;THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY WO2004/26846, 2004, A1 Location in patent:Page 54

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