Dimethyl Sulfoxide → tert-butyl N-[(2S)-1-oxo-3-phenylpropan-2-yl]carbamate

HRID 235511

Reaktionsgleichung

Reaktionsgleichung von HRID 235511
CS(C)=O.C(Cl)(=O)C(Cl)=O.[C:11]([NH:18][C@H:19]([CH2:27][OH:28])[CH2:20][C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)([O:13][C:14]([CH3:17])([CH3:16])[CH3:15])=[O:12].C(N(CC)CC)C>C(Cl)Cl>[C:11]([NH:18][C@H:19]([CH:27]=[O:28])[CH2:20][C:21]1[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=1)([O:13][C:14]([CH3:16])([CH3:15])[CH3:17])=[O:12]

Komponenten

6

Reaktionsbedingungen

Temperatur
-78 °C

Versuchsvorschrift

To dimethyl sulfoxide (2.82 mL, 39.8 mmol) dissolved in anhydrous methylene chloride (5 mL) and cooled to -78° C. was added dropwise oxalyl chloride (2.6 mL, 1.5 equiv). After 10 minutes at -78° C., N-Boc-Phenylalaninol (5.00 g, 19.9 mmol) dissolved in anhydrous methylene chloride (75 mL) was cannulated into the reaction mixture. After 15 minutes at -78° C., the reaction was stirred for 2 minutes at 0° C. and then cooled again to -78° C. Triethylamine (11.9 mL, 4.3 equiv) was added dropwise. After 25 minutes, the reaction was quenched with cooled 10% citric acid (15 mL) and then diluted with additional 10% citric acid (75 mL). Ether (300 mL) was added and the solution was washed with water (5×100 mL), brine, water (5×100 mL), and brine, dried over sodium sulfate, and concentrated under reduced pressure to afford the title compound (4.22 g).

Aufarbeitung

  1. waitAfter 15 minutes at -78° C.
  2. temperaturecooled again to -78° C
  3. waitAfter 25 minutes
  4. customthe reaction was quenched
  5. temperaturewith cooled 10% citric acid (15 mL)
  6. additiondiluted with additional 10% citric acid (75 mL)
  7. additionEther (300 mL) was added
  8. washthe solution was washed with water (5×100 mL), brine, water (5×100 mL), and brine
  9. dry with materialdried over sodium sulfate
  10. concentrationconcentrated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-828d80d34e2847fcbb40f93ca9596ed9
Quelldatensatz
uspto-grants-1997_01
Patentnummer
US05597926

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