Ammonia → (S)-2-amino-1-((S)-2,5-dihydrofuran-2-yl)ethanol

HRID 1665865

Reaction equation

HRID 1665865 reaction equation
[O:1]1[CH2:5][CH:4]=[CH:3][C@H:2]1[C@@H:6]([OH:19])[CH2:7][NH:8]C(=O)OCC1C=CC=CC=1.[Cl-].[NH4+].CC1C=CC(S(O[C@@H]2CO[C@@H]3[C@@H](Br)CO[C@H]23)(=O)=O)=CC=1.N>O.CC(O)C.[Zn].CO>[NH2:8][CH2:7][C@@H:6]([C@@H:2]1[CH:3]=[CH:4][CH2:5][O:1]1)[OH:19]

Participants

9

Conditions

Temperature
75 °C

Procedure

Alternative preparation of Benzyl (S)-2-((S)-2,5-dihydrofuran-2-yl)-2-hydroxyethylcarbamate (17); Zinc and ‘One-pot’ procedure. A solution of ammonium chloride (560 mg, 10.5 mmol) in water (7 mL) was added to a solution of bromotosylate (46) (2.86 g, 7.88 mmol) in propan-2-ol (14 mL) under argon. Zinc dust (560 mg, 8.67 mmol) was then added in portions over 4 minutes then the suspension stirred for 16 hours before filtering through celite in vacuo. The filter cake was washed with diethyl ether (60 mL). Hydrochloric acid (1M, 60 mL) was added to the filtrate then the organic phase separated. The aqueous layer was extracted with diethyl ether (60 mL) then the combined organic phase was washed with brine (60 mL), then dried (MgSO4), filtered and reduced in vacuo. The residue was dissolved in ammonium hydroxide (18 mL) and a solution of ammonia in propan-2-ol (12 mL, 2.0M, 24 mmol) then divided into three equal portions and heated in sealed tubes at 75° C. for 16 hours. The mixtures were combined using methanol then the solvents were removed in vacuo. The residue was azeotroped with diethyl ether (3×10 mL) to obtain (S)-2-amino-1-((S)-2,5-dihydrofuran-2-yl)ethanol which was used without further purification.

Workup

  1. filtrationbefore filtering through celite in vacuo
  2. washThe filter cake was washed with diethyl ether (60 mL)
  3. additionHydrochloric acid (1M, 60 mL) was added to the filtrate
  4. customthe organic phase separated
  5. extractionThe aqueous layer was extracted with diethyl ether (60 mL)
  6. washthe combined organic phase was washed with brine (60 mL)
  7. dry with materialdried (MgSO4)
  8. filtrationfiltered
  9. dissolutionThe residue was dissolved in ammonium hydroxide (18 mL)
  10. customthe solvents were removed in vacuo
  11. customThe residue was azeotroped with diethyl ether (3×10 mL)

Sources & evidence

ORD record
ord-17e110643eda437ba536b72dda6ef999
Source dataset
uspto-grants-2011_10
Patent number
US08039641B2

Linked notes

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