Sodium Thiosulfate → tert-Butyl N-(3-oxopropyl)carbamate

HRID 899738Notes

Reaction equation

HRID 899738 reaction equation
[OH:1][CH2:2][CH2:3][CH2:4][NH:5][C:6](=[O:12])[O:7][C:8]([CH3:11])([CH3:10])[CH3:9].CC(OI1(OC(C)=O)(OC(C)=O)OC(=O)C2C=CC=CC1=2)=O.[O-]S([O-])(=S)=O.[Na+].[Na+].C([O-])(O)=O.[Na+]>C(Cl)Cl.CCOCC>[C:8]([O:7][C:6]([NH:5][CH2:4][CH2:3][CH:2]=[O:1])=[O:12])([CH3:11])([CH3:10])[CH3:9]

Participants

7

Procedure

To a solution of tert-butyl N-(3-hydroxypropyl)carbamate (0.177 g, 1.01 mmol) in CH2Cl2 (5 mL) was added Dess-Martin periodinane (0.545 g, 1.28 mmol) and the resultant mixture was stirred at room temperature for 2.5 hours. The mixture was diluted with ether (20 mL) and treated with 20% aqueous Na2S2O3 (5 mL) and saturated aqueous NaHCO3 (5 mL). After 10 minutes the mixture became clear and colorless and the phases were separated. The aqueous phase was extracted with ether (3×10 mL). The combined organic extracts were washed sequentially with 20% aqueous Na2S2O3 (10 mL), saturated aqueous NaHCO3 (10 mL), and brine (10 mL), dried (MgSO4), and concentrated to provide 0.127 g (96%) of N-(tert-butoxycarbonyl)-3-amino-propionaldehyde as a colorless oil. 1H NMR (CDCl3) δ 1.43 (s, 9H), 2.71 (t, 2H, J=6.0 Hz), 3.42 (m, 2H), 4.89 (br s, 1H), 9.81 (s, 1H).

Workup

  1. customcolorless and the phases were separated
  2. extractionThe aqueous phase was extracted with ether (3×10 mL)
  3. washThe combined organic extracts were washed sequentially with 20% aqueous Na2S2O3 (10 mL), saturated aqueous NaHCO3 (10 mL), and brine (10 mL)
  4. dry with materialdried (MgSO4)
  5. concentrationconcentrated

Sources & evidence

ORD record
ord-f0d0e99b55e54485971defc7a9de15a2
Source dataset
uspto-grants-2008_04
Patent number
US07354934B2

Reaction notes

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