1,3-Difluoroacetone → HCID 67126718, compound
Reaction equation
[NH:1]1[CH2:4][CH:3]([NH:5]C(=O)OC(C)(C)C)[CH2:2]1.[F:13][CH2:14][C:15](=O)[CH2:16][F:17].C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>ClCCl>[F:13][CH2:14][CH:15]([N:1]1[CH2:2][CH:3]([NH2:5])[CH2:4]1)[CH2:16][F:17]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of tert-butyl azetidin-3-ylcarbamate (0.256 g) and 1,3-difluoropropan-2-one (0.154 g) in dichloromethane (2 mL) was added sodium triacetoxyborohydride (0.473 g) and the reaction was allowed to stirred at room temperature. After 16 hours, the reaction was quenched with saturated NaHCO3 solution (10 mL) and extracted into dichloromethane (25 mL). The organic layer was dried and concentrated. Silica gel chromatography (GraceResolv 12 g) eluting with a gradient of 0.5% to 3.5% methanol/dichloromethane followed by treatment with HCl (4.0M in dioxane, 3 mL) and methanol (0.5 mL) for 2 hours gave the title compound after concentration.
Workup
- customthe reaction was quenched with saturated NaHCO3 solution (10 mL)
- extractionextracted into dichloromethane (25 mL)
- customThe organic layer was dried
- concentrationconcentrated
- washSilica gel chromatography (GraceResolv 12 g) eluting with a gradient of 0.5% to 3.5% methanol/dichloromethane
- waitfollowed by treatment with HCl (4.0M in dioxane, 3 mL) and methanol (0.5 mL) for 2 hours
Sources & evidence
- ORD record
- ord-345560051a9b4515a1ab92c97f26ea1b
- Source dataset
- uspto-grants-2013_10
- Patent number
- US08546399B2
Reaction notes
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