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tert-Butyl bromoacetate → HCID 15896050, Verbindung

HRID 1738288
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1738288
[CH2:1]([NH:9][S:10]([C:13]1[CH:18]=[CH:17][C:16]([CH3:19])=[CH:15][CH:14]=1)(=[O:12])=[O:11])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].[Li+].C[Si]([N-][Si](C)(C)C)(C)C.Br[CH2:31][C:32]([O:34][C:35]([CH3:38])([CH3:37])[CH3:36])=[O:33]>C1COCC1.[NH4+].[Cl-].C(OCC)(=O)C>[C:35]([O:34][C:32](=[O:33])[CH2:31][N:9]([CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8])[S:10]([C:13]1[CH:18]=[CH:17][C:16]([CH3:19])=[CH:15][CH:14]=1)(=[O:11])=[O:12])([CH3:38])([CH3:37])[CH3:36]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 3

HCID 79177tert-Butyl bromoacetateHCID 2733832Lithium HexamethyldisilazideHCID 3090479Benzenesulfonamide, 4-methyl-N-octyl-

Produkt 1

HCID 15896050HCID 15896050, VerbindungAusbeute 53 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 8028TetrahydrofuranLösungsmittel2×
HCID 8857
Ethyl Acetate
Lösungsmittel
HCID 25517Ammonium ChlorideLösungsmittel

Reaktionsbedingungen

Temperatur
-78 °C

Versuchsvorschrift

N-Octyl-toluene-4-sulfonamide (7.0 g, 0.025 mol) was dissolved in dry THF (200 ml) and cooled to -78° C. A 1 M solution of LHMDS in THF (27.2 ml, 0.028 mol) was then added over 10 minutes. The reaction mixture was allowed to warm to -40° C. with stirring over 30 minutes. Neat tert-butyl bromoacetate (4.8 ml, 0.03 mol) was added over 5 minutes and the reaction mixture was allowed to warm to ambient temperature overnight. The reaction mixture was diluted with saturated aqueous NH4Cl (200 ml) and ethyl acetate (200 ml). The organic layer was separated and washed consecutively with 1 M HCl, 0.5M Na2CO3 and brine, dried over Na2SO4, filtered and concentrated in vacuo. The resulting crude oil was purified by flash chromatography (silica gel, 6% ethyl acetate in hexane) to give the title compound as a white solid (5.2 g, 53%). 1H NMR: δ (CDCl3), 7.72 (2H, d, J=8.3 Hz), 7.27 (2H, d, J=8.4 Hz), 3.94 (2H, s), 3.23 (2H, dd, J=7.5, 7.6 Hz), 2.42 (3H, s), 1.60-1.42 (2H, m), 1.39, (9H, s), 1.34-1.17 (10H, m), 0.88 (3H, t, J=6.9 Hz).

Aufarbeitung

  1. temperatureto warm to -40° C.
  2. temperatureto warm to ambient temperature overnight
  3. customThe organic layer was separated
  4. washwashed consecutively with 1 M HCl, 0.5M Na2CO3 and brine
  5. dry with materialdried over Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo
  8. customThe resulting crude oil was purified by flash chromatography (silica gel, 6% ethyl acetate in hexane)

Quellen und Nachweise

ORD-Eintrag
ord-95e0f4de06014e078a95762049b2ca1c
Quelldatensatz
uspto-grants-1999_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05962529

Notizen zur Reaktion

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