Acetone → (4S,5R)-4-(fluoromethyl)-5-(4-iodophenyl)-2,2-dimethyloxazolidine

HRID 2283169Notes

Reaction equation

HRID 2283169 reaction equation
[NH2:1][C@H:2]([CH2:12][F:13])[C@@H:3]([C:5]1[CH:10]=[CH:9][C:8]([I:11])=[CH:7][CH:6]=1)[OH:4].[CH3:14][C:15]([CH3:17])=O>>[F:13][CH2:12][C@@H:2]1[C@@H:3]([C:5]2[CH:10]=[CH:9][C:8]([I:11])=[CH:7][CH:6]=2)[O:4][C:15]([CH3:17])([CH3:14])[NH:1]1

Participants

3

Reactant 2

HCID 180AcetoneHCID 45257860(2S,1R)-2-Amino-3-fluoro-1-(4-iodo-phenyl)-propan-1-ol

Product 1

HCID 86695412(4S,5R)-4-(fluoromethyl)-5-(4-iodophenyl)-2,2-dimethyloxazolidine

Procedure

Commercially available (1R,2S)-2-amino-3-fluoro-1-(4-iodophenyl)propan-1-ol (6.0 g, 20.0 mmol) is dissolved in acetone (150 mL) and the mixture stirred at room temperature for 16 hours. The solvent is removed under reduced pressure to give the title compound (7.0 g). m/z (Cl) M+H 295.

Workup

  1. customThe solvent is removed under reduced pressure

Sources & evidence

ORD record
ord-9d520630afda4a13ba55bf85eb6b87e3
Source dataset
uspto-grants-2015_09
Patent number
US09145355B2

Reaction notes

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