Acetonitrile → [2-Chloro-6-(trimethylsilyl)benzoyl]ethylcarbamic acid, 1,1-dimethylethyl ester

HRID 2394881Notes

Reaction equation

HRID 2394881 reaction equation
[Cl:1][C:2]1[CH:12]=[CH:11][CH:10]=[C:9]([Si:13]([CH3:16])([CH3:15])[CH3:14])[C:3]=1[C:4](NCC)=[O:5].[C:17](=[O:28])([O:23][C:24]([CH3:27])([CH3:26])[CH3:25])OC(C)(C)C.[C:29](#[N:31])[CH3:30]>CN(C)C1C=CN=CC=1>[Cl:1][C:2]1[CH:12]=[CH:11][CH:10]=[C:9]([Si:13]([CH3:14])([CH3:15])[CH3:16])[C:3]=1[C:4]([CH2:30][CH2:29][NH:31][C:17](=[O:28])[O:23][C:24]([CH3:25])([CH3:26])[CH3:27])=[O:5]

Participants

5

Reactant 3

HCID 6342AcetonitrileHCID 10219638Carbonic acid, bis(1,1-dimethylethyl) ester3×HCID 186303792-Chloro-n-ethyl-6-(trimethylsilyl)benzamide

Product 1

HCID 57096133[2-Chloro-6-(trimethylsilyl)benzoyl]ethylcarbamic acid, 1,1-dimethylethyl ester

Reagents, catalysts & solvents 1

HCID 142844-(Dimethylamino)pyridineCatalyst

Procedure

To a solution of the compound of example 45 (3.83 g, 15 mmol) and di-t-butyl carbonate (3.60 g, 16.5 mmol) in acetonitrile was added 4-dimethylaminopyridine (0.18 g, 1.5 mmol). The solution was stirred at RT for 1 day, additional di-t-butyl carbonate (3.60 g) was added and stirring was continued for 3 days. Additional di-t-butyl carbonate (3.60 g) was added and the reaction was stirred overnight and concentrated. The residue was diluted with ether, washed with sat citric acid, sat NaHCO3, brine, dried (MgSO4) and concentrated to afford the title compound. The crude product was purified by flash chromatography (ethyl acetate /hexanes) and recrystallization from hexanes (-78° C.) to afford the title compound as a white solid (2.65 g, 50%). m.p. 51°-52° C.

Workup

  1. stirringstirring
  2. waitwas continued for 3 days
  3. stirringthe reaction was stirred overnight
  4. concentrationconcentrated
  5. additionThe residue was diluted with ether
  6. washwashed
  7. dry with materialdried (MgSO4)
  8. concentrationconcentrated

Sources & evidence

ORD record
ord-179f63dffb7e4ad3907d8725da8b2f35
Source dataset
uspto-grants-1998_09
Patent number
US05811411

Reaction notes

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