Reaktion #357254

ord-ba1e445f47844faaa2ea1eba40902c38

Reaktionsgleichung

CC(=O)Nc1cc(Cl)ccc1O
N-(5-chloro-2-hydroxyphenyl)acetamide
O=[N+]([O-])c1cccc(S(=O)(=O)OC[C@@H]2CO2)c1
(2S)-oxiran-2-ylmethyl3-nitrobenzenesulfonate
O=C([O-])[O-].[Cs+].[Cs+]
Cs2CO3
CC(=O)Nc1cc(Cl)ccc1OC[C@@H]1CO1
subtitled compound
Ausbeute 92.3%
CC(=O)Nc1cc(Cl)ccc1OC[C@@H]1CO1
N-{5-Chloro-2-[(2S)-oxiran-2-ylmethoxy]phenyl}acetamide
Ausbeute 92.3%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe reaction mixture was partitioned between ethyl acetate and water
  2. 2
    TrocknenThe organic layer was dried over Na2SO4
  3. 3
    Filtrationfiltered
  4. 4
    Einengenconcentrated
  5. 5
    SonstigeThe residue was purified by silica gel flash chromatography (0-50% ethyl acetate in petroleum ether)

Vorschrift

A mixture of N-(5-chloro-2-hydroxyphenyl)acetamide (500 mg, 2.69 mmol), (2S)-oxiran-2-ylmethyl3-nitrobenzenesulfonate (697 mg, 2.69 mmol) and Cs2CO3 (1.04 g, 3.22 mmol) in DMF (10 mL) was stirred at room temperature overnight. The reaction mixture was partitioned between ethyl acetate and water. The organic layer was dried over Na2SO4, filtered and concentrated. The residue was purified by silica gel flash chromatography (0-50% ethyl acetate in petroleum ether) to give the subtitled compound (600 mg).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07449475B2uspto-grants-2008_11