Di-tert-butyl dicarbonate → [1-(3,4-Difluorophenyl)-2hydroxy-propyl]-carbamic acid-tert-butyl ester

HRID 1167709Notes

Reaction equation

HRID 1167709 reaction equation
[NH2:1][CH2:2][C:3]([C:6]1[CH:11]=[CH:10][C:9]([F:12])=[C:8]([F:13])[CH:7]=1)([OH:5])[CH3:4].[NH2:14][C:15]([C:19]1[CH:24]=[CH:23][C:22]([F:25])=[C:21]([F:26])[CH:20]=1)(C)[CH2:16][OH:17].[C:27](O[C:35]([O:37][C:38]([CH3:41])([CH3:40])[CH3:39])=[O:36])([O:29][C:30]([CH3:33])([CH3:32])[CH3:31])=[O:28]>C(Cl)(Cl)Cl>[C:30]([O:29][C:27](=[O:28])[NH:1][CH2:2][C:3]([C:6]1[CH:11]=[CH:10][C:9]([F:12])=[C:8]([F:13])[CH:7]=1)([OH:5])[CH3:4])([CH3:33])([CH3:32])[CH3:31].[C:38]([O:37][C:35](=[O:36])[NH:14][CH:15]([C:19]1[CH:24]=[CH:23][C:22]([F:25])=[C:21]([F:26])[CH:20]=1)[CH:16]([OH:17])[CH3:2])([CH3:39])([CH3:40])[CH3:41]

Participants

6

Procedure

To a solution of 1-amino-2-(3,4-difluorophenyl)-propan-2-ol and 2-amino-2-(3,4-difluorophenyl)-propan-l-ol (1.2 g, 6.4 mmol) in CHCl3 (50 mL) at 0° C. was added a solution of di-tert-butyl dicarbonate (1.74 g, 7.9 mmol) in CHCl3 (10 mL) in one portion and the resulting solution was stirred overnight at room temperature. The solvent was removed in vacuo and the residue was subjected to column chromatography on silica gel (2:1 hexane-EtOAc followed by EtOAc) to obtain [2-(3,4-difluorophenyl)-2-hydroxy-propyl]-carbamic acid-tert-butyl ester and [1-(3,4-Difluorophenyl)-2-hydroxy-propyl]-carbamic acid-tert-butyl ester as a white solid (1.1 g, 60.1%).

Workup

  1. customThe solvent was removed in vacuo

Sources & evidence

ORD record
ord-a1768436cde84befad5260a3cac9911c
Source dataset
uspto-grants-2003_09
Patent number
US06620815B1

Reaction notes

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