3-Amino-1-propanol → HCID 43417613, compound
Reaction equation
[NH2:1][CH2:2][CH2:3][CH2:4][OH:5].[C:6]([CH2:10][C:11](Cl)=[O:12])([CH3:9])([CH3:8])[CH3:7]>ClCCl>[OH:5][CH2:4][CH2:3][CH2:2][NH:1][C:11](=[O:12])[CH2:10][C:6]([CH3:9])([CH3:8])[CH3:7]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 0 °C
Procedure
3-Amino-1-propanol (6.0 mL, 0.078 mol) was dissolved in dichloromethane (68 mL) then cooled at 0° C. A solution of tert-butylacetyl chloride (2.7 mL, 0.020 mol) in dichloromethane (25 mL) was added dropwise over 10 min. The reaction mixture was stirred for 1 h then concentrated to dryness. The residue was dissolved in EtOAC (100 mL) and washed with brine (3×). The organic extract was dried over Na2SO4, filtered, and concentrated to dryness to give the title compound as a clear oil (3.1 g, 91% yield). 1H NMR (DMSO, 400 mHz) δ (ppm): 7.64 (bs, 1H), 4.36 (t, J=5.3 Hz, 1H), 3.38-3.33 (m, 2H), 3.02 (q, J=6.8 Hz, 2H), 1.88 (s, 2H), 1.52-1.45 (m, 2H), 0.90 (s, 9H).
Workup
- concentrationthen concentrated to dryness
- dissolutionThe residue was dissolved in EtOAC (100 mL)
- washwashed with brine (3×)
- extractionThe organic extract
- dry with materialwas dried over Na2SO4
- filtrationfiltered
- concentrationconcentrated to dryness
Sources & evidence
- ORD record
- ord-89aaf0bde8eb4c0f97b5fd658190493d
- Source dataset
- uspto-grants-2015_02
- Patent number
- US08952031B2
Reaction notes
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