Water → HCID 59487509, compound
Reaction equation
[N:1]([CH2:4][C:5]([OH:22])([C:18]([F:21])([F:20])[F:19])[CH2:6][NH:7][C:8](=[O:17])[C:9]1[C:14]([Cl:15])=[CH:13][CH:12]=[CH:11][C:10]=1[Cl:16])=[N+]=[N-].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.O>O1CCCC1>[NH2:1][CH2:4][C:5]([OH:22])([C:18]([F:21])([F:19])[F:20])[CH2:6][NH:7][C:8](=[O:17])[C:9]1[C:14]([Cl:15])=[CH:13][CH:12]=[CH:11][C:10]=1[Cl:16]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A stirred solution of N-[2-(azidomethyl)-3,3,3-trifluoro-2-hydroxypropyl]-2,6-dichlorobenzamide (0.06 g) in dry tetrahydrofuran (30 ml) was treated with polymer bound triphenylphosphine (3 mmol/g, 2.01 g). The mixture was vigorously stirred at room temperature for 19 hours before water (3 ml) was added. Stirring was continued at room temperature for a further 24 hours. The suspension was then diluted with tetrahydrofuran (50 ml) and then filtered through a pad of hyflo. The pad was washed with further tetrahydrofuran (2×30 ml). The combined filtrate and washings were partitioned between ethyl acetate (100 ml) and water (50 ml). The separated organic phase was further washed with water (2×50 ml), passed through a hydrophobic frit and concentrated in vacuo and then re-evaporated in vacuo with ethanol (1×20 ml) to give the title compound (0.84 g) as a near colourless gum.
Workup
- additionwas added
- filtrationfiltered through a pad of hyflo
- washThe pad was washed with further tetrahydrofuran (2×30 ml)
- customThe combined filtrate and washings were partitioned between ethyl acetate (100 ml) and water (50 ml)
- washThe separated organic phase was further washed with water (2×50 ml)
- concentrationconcentrated in vacuo
- customre-evaporated in vacuo with ethanol (1×20 ml)
Sources & evidence
- ORD record
- ord-5ee86b7080584641a3eb5fe6f81f7377
- Source dataset
- uspto-grants-2012_08
- Patent number
- US08247377B2
Reaction notes
Loading…