Borane → HCID 178419237, Verbindung

HRID 258137

Reaktionsgleichung

Reaktionsgleichung von HRID 258137
[C:1]1([C:7]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)([C@@H:9]2[CH2:13][CH2:12][CH2:11][NH:10]2)[OH:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.CSC.[BH3:23].B>C1(C)C=CC=CC=1>[C:1]1([C:7]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)([CH:9]2[CH2:13][CH2:12][CH2:11][NH:10]2)[OH:8])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1.[BH3:23]

Komponenten

5

Reaktionsbedingungen

Temperatur
20 °C

Versuchsvorschrift

A 250-mL three-necked flask fitted with a mechanical stirrer, nitrogen inlet tube, and teflon coated thermocouple probe, was charged with a solution of the free base product of Example 1 Step B (20.7 g, 81.7 mmol) in dry toluene (100 mL). To the stirred solution at 20° C. was added borane-dimethyl sulfide (10M, 10.0 mL, 100 mmol) over 5 minutes via syringe. The borane reacted immediately in an exothermic reaction (raising the internal temperature from 20° C. to 32° C.) forming a thick white precipitate. With continued stirring, the mixture was allowed to cool to room temperature (20° C.) over a 1 hour period. The mixture was filtered, and the product cake washed with dry toluene (25 mL). The product was dried in vacuo (20° C., 0.01 mBar) to constant weight. Yield 15.7 g (72%) of a white crystal line solid. m.p. 130°-132° C. (dec). 1H NMR (CDCl3 ) δ7.7-7.1 (m, 10 H, Ar-H), 5.15 (s, 1 H, --OH), 4.5 (br, 1 H, --NH), 4.2 (m, 1 H, C2-H), 3.25 (m, 2 H, C5-H2), 2.6 (m, 1 H, C4- H), 2.3 (m, 1 H, C4-H), 1.85 (m, 1 H, C3-H), 1.6 (m, 1 H, C3-H), 2.1-0.7 (br, 3 H, BH3). 13C NMR (CDCl3) δ145.8, 144.5 (C1', C1"), 129.1, 128.2 (C3', C5', C3", C5"), 127.4, 127.0 (C4', C4"), 125.2, 125.1 (C2', C6', C2", C6"), 76.5 (Cα), 69.6 (C2), 55.6 (C 5), 20.6 (C4), 19.9 (C3).

Aufarbeitung

  1. customA 250-mL three-necked flask fitted with a mechanical stirrer, nitrogen inlet tube
  2. temperatureraising the internal temperature from 20° C. to 32° C.)
  3. customforming a thick white precipitate
  4. filtrationThe mixture was filtered
  5. washthe product cake washed with dry toluene (25 mL)
  6. customThe product was dried in vacuo (20° C., 0.01 mBar) to constant weight

Quellen und Nachweise

ORD-Eintrag
ord-969b93af375048c4b3dc8543aaf96b43
Quelldatensatz
uspto-grants-1993_11
Patentnummer
US05264585

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